rs587777529

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs587777529(A;A)

Make rs587777529(A;C)

Reference

GRCh38 38.1/142

Chromosome

11

Position

64739431

Gene

RASGRP2

is a	snp
is	mentioned by
dbSNP	rs587777529
dbSNP (classic)	rs587777529
ClinGen	rs587777529
ebi	rs587777529
HLI	rs587777529
Exac	rs587777529
Gnomad	rs587777529
Varsome	rs587777529
LitVar	rs587777529
Map	rs587777529
PheGenI	rs587777529
Biobank	rs587777529
1000 genomes	rs587777529
hgdp	rs587777529
ensembl	rs587777529
geneview	rs587777529
scholar	rs587777529
google	rs587777529
pharmgkb	rs587777529
gwascentral	rs587777529
openSNP	rs587777529
23andMe	rs587777529
SNPshot	rs587777529
SNPdbe	rs587777529
MSV3d	rs587777529
GWAS Ctlg	rs587777529

Max Magnitude

0

ClinVar
Risk	rs587777529(A;A) rs587777529(T;T)
Alt	rs587777529(A;A) rs587777529(T;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 UniProtKB (protein)
CLNACC	RCV000128611.2,