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rs137853067

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853067(C;T)
Make rs137853067(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160041938
GeneKCNJ10
is asnp
is mentioned by
dbSNPrs137853067
ebirs137853067
HLIrs137853067
Exacrs137853067
Varsomers137853067
Maprs137853067
PheGenIrs137853067
hapmaprs137853067
1000 genomesrs137853067
hgdprs137853067
ensemblrs137853067
gopubmedrs137853067
geneviewrs137853067
scholarrs137853067
googlers137853067
pharmgkbrs137853067
gwascentralrs137853067
openSNPrs137853067
23andMers137853067
23andMe allrs137853067
SNP Nexus

SNPshotrs137853067
SNPdbers137853067
MSV3drs137853067
GWAS Ctlgrs137853067
Max Magnitude0
OMIM602208
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853067(T;T)
Alt rs137853067(T;T)
Reference rs137853067(C;C)
Significance Pathogenic
Disease SeSAME syndrome
Variation info
Gene KCNJ10
CLNDBN SeSAME syndrome
Reversed 1
HGVS NC_000001.10:g.160011728G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007889.4,