chr11:86157598:T>C Detail (hg38)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:85,868,640-85,868,640 View the variant detail on this assembly version. |
hg38 | chr11:86,157,598-86,157,598 |
HGVS
[No Data.]
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.593 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | obesity | (2) Four additional AD risk SNPs were nominally associated with obesity (rs17125... | BeFree | 24788522 | Detail |
<0.001 | obesity | (2) Four additional AD risk SNPs were nominally associated with obesity (rs17125... | BeFree | 24788522 | Detail |
<0.001 | obesity | (2) Four additional AD risk SNPs were nominally associated with obesity (rs17125... | BeFree | 24788522 | Detail |
0.196 | obesity | (2) Four additional AD risk SNPs were nominally associated with obesity (rs17125... | BeFree | 24788522 | Detail |
0.002 | Alzheimer Disease, Late Onset | PICALM-rs3851179-G had an unexpected protective effect on incident MCI/LOAD. | BeFree | 25189118 | Detail |
0.269 | Alzheimer's disease | [Genome-wide association study identifies variants at CLU and PICALM associated ... | GAD | 19734902 | Detail |
<0.001 | Mild cognitive disorder | PICALM-rs3851179-G had an unexpected protective effect on incident MCI/LOAD. | BeFree | 25189118 | Detail |
0.003 | schizophrenia | Association analysis between the rs11136000 single nucleotide polymorphism in cl... | BeFree | 20738160 | Detail |
0.287 | Alzheimer's disease | In addition, the rs541458 and rs3851179 of PICALM SNPs are not related to develo... | BeFree | 26434199 | Detail |
0.262 | Alzheimer's disease | We investigated the influence of the rs6656401 single nucleotide polymorphisms (... | BeFree | 23650005 | Detail |
0.269 | Alzheimer's disease | In addition, the rs541458 and rs3851179 of PICALM SNPs are not related to develo... | BeFree | 26434199 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
(2) Four additional AD risk SNPs were nominally associated with obesity (rs17125944 at FERMT2, pBMI ... | DisGeNET | Detail |
(2) Four additional AD risk SNPs were nominally associated with obesity (rs17125944 at FERMT2, pBMI ... | DisGeNET | Detail |
(2) Four additional AD risk SNPs were nominally associated with obesity (rs17125944 at FERMT2, pBMI ... | DisGeNET | Detail |
(2) Four additional AD risk SNPs were nominally associated with obesity (rs17125944 at FERMT2, pBMI ... | DisGeNET | Detail |
PICALM-rs3851179-G had an unexpected protective effect on incident MCI/LOAD. | DisGeNET | Detail |
[Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer\'s di... | DisGeNET | Detail |
PICALM-rs3851179-G had an unexpected protective effect on incident MCI/LOAD. | DisGeNET | Detail |
Association analysis between the rs11136000 single nucleotide polymorphism in clusterin gene, rs3851... | DisGeNET | Detail |
In addition, the rs541458 and rs3851179 of PICALM SNPs are not related to development of BPSD, but t... | DisGeNET | Detail |
We investigated the influence of the rs6656401 single nucleotide polymorphisms (SNP) of the CR1 gene... | DisGeNET | Detail |
In addition, the rs541458 and rs3851179 of PICALM SNPs are not related to development of BPSD, but t... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs3851179 dbSNP
- Genome
- hg38
- Position
- chr11:86,157,598-86,157,598
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs3851179
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.5928
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 9934
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16758
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