rs587776702

Orientation

plus

Stabilized

plus

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

Make rs587776702(-;-)

Make rs587776702(-;AGC)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

3898082

Gene

P2RX1

is a	snp
is	mentioned by
dbSNP	rs587776702
dbSNP (classic)	rs587776702
ClinGen	rs587776702
ebi	rs587776702
HLI	rs587776702
Exac	rs587776702
Gnomad	rs587776702
Varsome	rs587776702
LitVar	rs587776702
Map	rs587776702
PheGenI	rs587776702
Biobank	rs587776702
1000 genomes	rs587776702
hgdp	rs587776702
ensembl	rs587776702
geneview	rs587776702
scholar	rs587776702
google	rs587776702
pharmgkb	rs587776702
gwascentral	rs587776702
openSNP	rs587776702
23andMe	rs587776702
SNPshot	rs587776702
SNPdbe	rs587776702
MSV3d	rs587776702
GWAS Ctlg	rs587776702

Max Magnitude

0

ClinVar
Risk	rs587776702(-;-)
Alt	rs587776702(-;-)
Reference	Rs587776702(AGC;AGC)
Significance	Pathogenic
Disease	Platelet-type bleeding disorder 8
Variation	info
Gene	P2RX1
CLNDBN	Platelet-type bleeding disorder 8
Reversed	0
HGVS	NC_000017.10:g.3801376_3801378delAGC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009293.4,