chr13:113121768:C>T Detail (hg38)

Information

Genome

Assembly Position
hg19 chr13:113,776,082-113,776,082 View the variant detail on this assembly version.
hg38 chr13:113,121,768-113,121,768

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.081
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 Cerebrovascular accident Among whites, six SNPs were associated with stroke, with a nominal P-value of &l... BeFree 21114618 Detail
<0.001 Cerebrovascular accident Among whites, six SNPs were associated with stroke, with a nominal P-value of &l... BeFree 21114618 Detail
Annotation

Annotations

DescrptionSourceLinks
Among whites, six SNPs were associated with stroke, with a nominal P-value of &lt; 0.01: rs6046 and ... DisGeNET Detail
Among whites, six SNPs were associated with stroke, with a nominal P-value of &lt; 0.01: rs6046 and ... DisGeNET Detail
Gene
-
dbSNP
rs3093261 dbSNP
Genome
hg38
Position
chr13:113,121,768-113,121,768
Variant Type
snv
Reference Allele
C
Alternative Allele
T
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))
rs3093261
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.0811
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
1359
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16758
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