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

rs375607980

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs375607980(G;G)
Make rs375607980(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47349875
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs375607980
ebirs375607980
HLIrs375607980
Exacrs375607980
Varsomers375607980
Maprs375607980
PheGenIrs375607980
hapmaprs375607980
1000 genomesrs375607980
hgdprs375607980
ensemblrs375607980
gopubmedrs375607980
geneviewrs375607980
scholarrs375607980
googlers375607980
pharmgkbrs375607980
gwascentralrs375607980
openSNPrs375607980
23andMers375607980
23andMe allrs375607980
SNP Nexus

SNPshotrs375607980
SNPdbers375607980
MSV3drs375607980
GWAS Ctlgrs375607980
Max Magnitude0
ClinVar
Risk rs375607980(A,G;A,G)
Alt rs375607980(A,G;A,G)
Reference rs375607980(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47371426T>A
CLNSRC
CLNACC RCV000158293.1,