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rs137853197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853197(A;G)
Make rs137853197(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position77942756
GeneNEXN
is asnp
is mentioned by
dbSNPrs137853197
ebirs137853197
HLIrs137853197
Exacrs137853197
Varsomers137853197
Maprs137853197
PheGenIrs137853197
hapmaprs137853197
1000 genomesrs137853197
hgdprs137853197
ensemblrs137853197
gopubmedrs137853197
geneviewrs137853197
scholarrs137853197
googlers137853197
pharmgkbrs137853197
gwascentralrs137853197
openSNPrs137853197
23andMers137853197
23andMe allrs137853197
SNP Nexus

SNPshotrs137853197
SNPdbers137853197
MSV3drs137853197
GWAS Ctlgrs137853197
Max Magnitude0
OMIM613121
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853197(G;G)
Alt rs137853197(G;G)
Reference rs137853197(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 1CC not specified not provided Primary dilated cardiomyopathy Familial hypertrophic cardiomyopathy 20
Variation info
Gene NEXN
CLNDBN Dilated cardiomyopathy 1CC not specified not provided Primary dilated cardiomyopathy Familial hypertrophic cardiomyopathy 20
Reversed 0
HGVS NC_000001.10:g.78408441A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000354.2, RCV000041170.2, RCV000183674.2, RCV000208290.1, RCV000234084.1,