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rs387906919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906919(A;A)
Make rs387906919(A;G)
ReferenceGRCh37.p10 37.5/138
Chromosome19
Position55539032
GeneGP6
is asnp
is mentioned by
dbSNPrs387906919
ebirs387906919
HLIrs387906919
Exacrs387906919
Varsomers387906919
Maprs387906919
PheGenIrs387906919
hapmaprs387906919
1000 genomesrs387906919
hgdprs387906919
ensemblrs387906919
gopubmedrs387906919
geneviewrs387906919
scholarrs387906919
googlers387906919
pharmgkbrs387906919
gwascentralrs387906919
openSNPrs387906919
23andMers387906919
23andMe allrs387906919
SNP Nexus

SNPshotrs387906919
SNPdbers387906919
MSV3drs387906919
GWAS Ctlgrs387906919
Max Magnitude0
ClinVar
Risk rs387906919(A,T;A,T)
Alt rs387906919(A,T;A,T)
Reference rs387906919(G;G)
Significance Pathogenic
Disease Platelet-type bleeding disorder 11
Variation info
Gene GP6
CLNDBN Platelet-type bleeding disorder 11
Reversed 1
HGVS NC_000019.9:g.55539032C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023462.3,