Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519503

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519503(A;A)
Make rs1057519503(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position74789339
GeneNCF1
is asnp
is mentioned by
dbSNPrs1057519503
dbSNP (old)rs1057519503
ClinGenrs1057519503
ebirs1057519503
HLIrs1057519503
Exacrs1057519503
Gnomadrs1057519503
Varsomers1057519503
Maprs1057519503
PheGenIrs1057519503
Biobankrs1057519503
1000 genomesrs1057519503
hgdprs1057519503
ensemblrs1057519503
gopubmedrs1057519503
geneviewrs1057519503
scholarrs1057519503
googlers1057519503
pharmgkbrs1057519503
gwascentralrs1057519503
openSNPrs1057519503
23andMers1057519503
23andMe allrs1057519503
SNPshotrs1057519503
SNPdbers1057519503
MSV3drs1057519503
GWAS Ctlgrs1057519503
Max Magnitude0
ClinVar
Risk rs1057519503(A;A)
Alt rs1057519503(A;A)
Reference Rs1057519503(G;G)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 4
Variation info
Gene NCF1
CLNDBN Familial hypertrophic cardiomyopathy 4
Reversed 0
HGVS NC_000007.13:g.74203683G>A
CLNSRC
CLNACC RCV000416494.1,