chr2:634905:T>C Detail (hg19)

Information

Genome

Assembly Position
hg19 chr2:634,905-634,905
hg38 chr2:634,905-634,905 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.906
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance risk factor
Review star
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
risk factor 2019-12-26 no assertion criteria provided obesity unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.400 obesity Using the three obesity-associated polymorphisms FTO rs9939609, MC4R rs17782313,... BeFree 24762112 Detail
<0.001 diabetes mellitus We tested the hypothesis that the ADRB2rs1800888(Thr164Ile) polymorphism associa... BeFree 22466342 Detail
<0.001 Diabetes We tested the hypothesis that the ADRB2rs1800888(Thr164Ile) polymorphism associa... BeFree 22466342 Detail
0.151 obesity Using the three obesity-associated polymorphisms FTO rs9939609, MC4R rs17782313,... BeFree 24762112 Detail
0.162 obesity The SNP rs10913469 in SEC16B (P=0.000012) and four SNPs (rs2867125, rs6548238, r... BeFree 19851340 Detail
Annotation

Annotations

DescrptionSourceLinks
NC_000002.12:g.634905T>C AND Obesity ClinVar Detail
Using the three obesity-associated polymorphisms FTO rs9939609, MC4R rs17782313, and TMEM18 rs654823... DisGeNET Detail
We tested the hypothesis that the ADRB2rs1800888(Thr164Ile) polymorphism associates with risk of obe... DisGeNET Detail
We tested the hypothesis that the ADRB2rs1800888(Thr164Ile) polymorphism associates with risk of obe... DisGeNET Detail
Using the three obesity-associated polymorphisms FTO rs9939609, MC4R rs17782313, and TMEM18 rs654823... DisGeNET Detail
The SNP rs10913469 in SEC16B (P=0.000012) and four SNPs (rs2867125, rs6548238, rs4854344 and rs75613... DisGeNET Detail
Gene
-
dbSNP
rs6548238 dbSNP
Genome
hg19
Position
chr2:634,905-634,905
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))
rs6548238
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.9056
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
15178
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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