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rs137853073

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853073(A;A)
Make rs137853073(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position160041952
GeneKCNJ10
is asnp
is mentioned by
dbSNPrs137853073
ebirs137853073
HLIrs137853073
Exacrs137853073
Varsomers137853073
Maprs137853073
PheGenIrs137853073
hapmaprs137853073
1000 genomesrs137853073
hgdprs137853073
ensemblrs137853073
gopubmedrs137853073
geneviewrs137853073
scholarrs137853073
googlers137853073
pharmgkbrs137853073
gwascentralrs137853073
openSNPrs137853073
23andMers137853073
23andMe allrs137853073
SNP Nexus

SNPshotrs137853073
SNPdbers137853073
MSV3drs137853073
GWAS Ctlgrs137853073
Max Magnitude0
OMIM602208
Desc
Variant0008
Relatedalso
ClinVar
Risk rs137853073(A;A)
Alt rs137853073(A;A)
Reference rs137853073(C;C)
Significance Pathogenic
Disease Enlarged vestibular aqueduct syndrome
Variation info
Gene KCNJ10
CLNDBN Enlarged vestibular aqueduct syndrome
Reversed 1
HGVS NC_000001.10:g.160011742G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007895.3,