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rs786205565

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205565(C;G)
Make rs786205565(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position101319817
GeneIMPG2
is asnp
is mentioned by
dbSNPrs786205565
ebirs786205565
HLIrs786205565
Exacrs786205565
Varsomers786205565
Maprs786205565
PheGenIrs786205565
hapmaprs786205565
1000 genomesrs786205565
hgdprs786205565
ensemblrs786205565
gopubmedrs786205565
geneviewrs786205565
scholarrs786205565
googlers786205565
pharmgkbrs786205565
gwascentralrs786205565
openSNPrs786205565
23andMers786205565
23andMe allrs786205565
SNP Nexus

SNPshotrs786205565
SNPdbers786205565
MSV3drs786205565
GWAS Ctlgrs786205565
Max Magnitude0
ClinVar
Risk rs786205565(G;G)
Alt rs786205565(G;G)
Reference rs786205565(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IMPG2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.101038661G>C
CLNSRC
CLNACC RCV000171369.1,