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rs763295314

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs763295314(A;C)
Make rs763295314(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position101291499
GeneIMPG2
is asnp
is mentioned by
dbSNPrs763295314
ebirs763295314
HLIrs763295314
Exacrs763295314
Varsomers763295314
Maprs763295314
PheGenIrs763295314
hapmaprs763295314
1000 genomesrs763295314
hgdprs763295314
ensemblrs763295314
gopubmedrs763295314
geneviewrs763295314
scholarrs763295314
googlers763295314
pharmgkbrs763295314
gwascentralrs763295314
openSNPrs763295314
23andMers763295314
23andMe allrs763295314
SNP Nexus

SNPshotrs763295314
SNPdbers763295314
MSV3drs763295314
GWAS Ctlgrs763295314
Max Magnitude0
ClinVar
Risk rs763295314(C;C)
Alt rs763295314(C;C)
Reference rs763295314(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IMPG2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.101010343A>C
CLNSRC
CLNACC RCV000171367.1,