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rs772372530

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772372530(-;-)
Make rs772372530(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position108922447
GeneGPSM2
is asnp
is mentioned by
dbSNPrs772372530
ebirs772372530
HLIrs772372530
Exacrs772372530
Varsomers772372530
Maprs772372530
PheGenIrs772372530
hapmaprs772372530
1000 genomesrs772372530
hgdprs772372530
ensemblrs772372530
gopubmedrs772372530
geneviewrs772372530
scholarrs772372530
googlers772372530
pharmgkbrs772372530
gwascentralrs772372530
openSNPrs772372530
23andMers772372530
23andMe allrs772372530
SNP Nexus

SNPshotrs772372530
SNPdbers772372530
MSV3drs772372530
GWAS Ctlgrs772372530
Max Magnitude0
ClinVar
Risk rs772372530(;)
Alt rs772372530(;)
Reference rs772372530(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GPSM2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.109465069delG
CLNSRC
CLNACC RCV000224236.1,