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rs146245480

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146245480(C;T)
Make rs146245480(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position77926863
GeneNEXN
is asnp
is mentioned by
dbSNPrs146245480
ebirs146245480
HLIrs146245480
Exacrs146245480
Varsomers146245480
Maprs146245480
PheGenIrs146245480
hapmaprs146245480
1000 genomesrs146245480
hgdprs146245480
ensemblrs146245480
gopubmedrs146245480
geneviewrs146245480
scholarrs146245480
googlers146245480
pharmgkbrs146245480
gwascentralrs146245480
openSNPrs146245480
23andMers146245480
23andMe allrs146245480
SNP Nexus

SNPshotrs146245480
SNPdbers146245480
MSV3drs146245480
GWAS Ctlgrs146245480
Max Magnitude0
ClinVar
Risk rs146245480(A,T;A,T)
Alt rs146245480(A,T;A,T)
Reference rs146245480(C;C)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 20 not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene NEXN
CLNDBN Familial hypertrophic cardiomyopathy 20 not specified Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.78392548C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023985.2, RCV000041184.2, RCV000143936.1,