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rs137853198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853198(A;A)
Make rs137853198(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position77942632
GeneNEXN
is asnp
is mentioned by
dbSNPrs137853198
ebirs137853198
HLIrs137853198
Exacrs137853198
Varsomers137853198
Maprs137853198
PheGenIrs137853198
hapmaprs137853198
1000 genomesrs137853198
hgdprs137853198
ensemblrs137853198
gopubmedrs137853198
geneviewrs137853198
scholarrs137853198
googlers137853198
pharmgkbrs137853198
gwascentralrs137853198
openSNPrs137853198
23andMers137853198
23andMe allrs137853198
SNP Nexus

SNPshotrs137853198
SNPdbers137853198
MSV3drs137853198
GWAS Ctlgrs137853198
Max Magnitude0
OMIM613121
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853198(A;A)
Alt rs137853198(A;A)
Reference rs137853198(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1CC
Variation info
Gene NEXN
CLNDBN Dilated cardiomyopathy 1CC
Reversed 0
HGVS NC_000001.10:g.78408317C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000355.2,