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rs145387010

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145387010(A;A)
Make rs145387010(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position90918950
GeneANKRD1
is asnp
is mentioned by
dbSNPrs145387010
ebirs145387010
HLIrs145387010
Exacrs145387010
Varsomers145387010
Maprs145387010
PheGenIrs145387010
hapmaprs145387010
1000 genomesrs145387010
hgdprs145387010
ensemblrs145387010
gopubmedrs145387010
geneviewrs145387010
scholarrs145387010
googlers145387010
pharmgkbrs145387010
gwascentralrs145387010
openSNPrs145387010
23andMers145387010
23andMe allrs145387010
SNP Nexus

SNPshotrs145387010
SNPdbers145387010
MSV3drs145387010
GWAS Ctlgrs145387010
Max Magnitude0
ClinVar
Risk rs145387010(A;A)
Alt rs145387010(A;A)
Reference rs145387010(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided not specified
Variation info
Gene ANKRD1
CLNDBN Primary familial hypertrophic cardiomyopathy not provided not specified
Reversed 0
HGVS NC_000010.10:g.92678707G>A
CLNSRC
CLNACC RCV000171828.1, RCV000178292.1, RCV000183297.2,