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rs587777529

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777529(A;A)
Make rs587777529(A;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position64739431
GeneRASGRP2
is asnp
is mentioned by
dbSNPrs587777529
ebirs587777529
HLIrs587777529
Exacrs587777529
Varsomers587777529
Maprs587777529
PheGenIrs587777529
hapmaprs587777529
1000 genomesrs587777529
hgdprs587777529
ensemblrs587777529
gopubmedrs587777529
geneviewrs587777529
scholarrs587777529
googlers587777529
pharmgkbrs587777529
gwascentralrs587777529
openSNPrs587777529
23andMers587777529
23andMe allrs587777529
SNP Nexus

SNPshotrs587777529
SNPdbers587777529
MSV3drs587777529
GWAS Ctlgrs587777529
Max Magnitude0
ClinVar
Risk rs587777529(A,T;A,T)
Alt rs587777529(A,T;A,T)
Reference rs587777529(C;C)
Significance Pathogenic
Disease Platelet-type bleeding disorder 18
Variation info
Gene RASGRP2
CLNDBN Platelet-type bleeding disorder 18
Reversed 0
HGVS NC_000011.9:g.64506903C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128611.2,