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rs137853066

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853066(C;C)
Make rs137853066(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position160042339
GeneKCNJ10
is asnp
is mentioned by
dbSNPrs137853066
ebirs137853066
HLIrs137853066
Exacrs137853066
Varsomers137853066
Maprs137853066
PheGenIrs137853066
hapmaprs137853066
1000 genomesrs137853066
hgdprs137853066
ensemblrs137853066
gopubmedrs137853066
geneviewrs137853066
scholarrs137853066
googlers137853066
pharmgkbrs137853066
gwascentralrs137853066
openSNPrs137853066
23andMers137853066
23andMe allrs137853066
SNP Nexus

SNPshotrs137853066
SNPdbers137853066
MSV3drs137853066
GWAS Ctlgrs137853066
Max Magnitude0
OMIM602208
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853066(A,C;A,C)
Alt rs137853066(A,C;A,C)
Reference rs137853066(G;G)
Significance Pathogenic
Disease SeSAME syndrome
Variation info
Gene KCNJ10
CLNDBN SeSAME syndrome
Reversed 1
HGVS NC_000001.10:g.160012129C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007888.3,