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rs587776702

From SNPedia

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Geno Mag Summary
(AGC;AGC) 0 common in clinvar
Make rs587776702(-;-)
Make rs587776702(-;AGC)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position3898082
GeneP2RX1
is asnp
is mentioned by
dbSNPrs587776702
ebirs587776702
HLIrs587776702
Exacrs587776702
Varsomers587776702
Maprs587776702
PheGenIrs587776702
hapmaprs587776702
1000 genomesrs587776702
hgdprs587776702
ensemblrs587776702
gopubmedrs587776702
geneviewrs587776702
scholarrs587776702
googlers587776702
pharmgkbrs587776702
gwascentralrs587776702
openSNPrs587776702
23andMers587776702
23andMe allrs587776702
SNP Nexus

SNPshotrs587776702
SNPdbers587776702
MSV3drs587776702
GWAS Ctlgrs587776702
Max Magnitude0
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,