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rs112179534

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs112179534(G;G)
Make rs112179534(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341246
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs112179534
ebirs112179534
HLIrs112179534
Exacrs112179534
Varsomers112179534
Maprs112179534
PheGenIrs112179534
hapmaprs112179534
1000 genomesrs112179534
hgdprs112179534
ensemblrs112179534
gopubmedrs112179534
geneviewrs112179534
scholarrs112179534
googlers112179534
pharmgkbrs112179534
gwascentralrs112179534
openSNPrs112179534
23andMers112179534
23andMe allrs112179534
SNP Nexus

SNPshotrs112179534
SNPdbers112179534
MSV3drs112179534
GWAS Ctlgrs112179534
Max Magnitude0
ClinVar
Risk rs112179534(G;G)
Alt rs112179534(G;G)
Reference rs112179534(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47362797T>G
CLNSRC
CLNACC RCV000158116.1,