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rs137853071

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853071(C;T)
Make rs137853071(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position160041644
GeneKCNJ10
is asnp
is mentioned by
dbSNPrs137853071
ebirs137853071
HLIrs137853071
Exacrs137853071
Varsomers137853071
Maprs137853071
PheGenIrs137853071
hapmaprs137853071
1000 genomesrs137853071
hgdprs137853071
ensemblrs137853071
gopubmedrs137853071
geneviewrs137853071
scholarrs137853071
googlers137853071
pharmgkbrs137853071
gwascentralrs137853071
openSNPrs137853071
23andMers137853071
23andMe allrs137853071
SNP Nexus

SNPshotrs137853071
SNPdbers137853071
MSV3drs137853071
GWAS Ctlgrs137853071
Max Magnitude0
OMIM602208
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137853071(T;T)
Alt rs137853071(T;T)
Reference rs137853071(C;C)
Significance Pathogenic
Disease SeSAME syndrome
Variation info
Gene KCNJ10
CLNDBN SeSAME syndrome
Reversed 1
HGVS NC_000001.10:g.160011434G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007893.4,