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rs786205564

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205564(A;A)
Make rs786205564(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position101244057
GeneIMPG2
is asnp
is mentioned by
dbSNPrs786205564
ebirs786205564
HLIrs786205564
Exacrs786205564
Varsomers786205564
Maprs786205564
PheGenIrs786205564
hapmaprs786205564
1000 genomesrs786205564
hgdprs786205564
ensemblrs786205564
gopubmedrs786205564
geneviewrs786205564
scholarrs786205564
googlers786205564
pharmgkbrs786205564
gwascentralrs786205564
openSNPrs786205564
23andMers786205564
23andMe allrs786205564
SNP Nexus

SNPshotrs786205564
SNPdbers786205564
MSV3drs786205564
GWAS Ctlgrs786205564
Max Magnitude0
ClinVar
Risk rs786205564(A;A)
Alt rs786205564(A;A)
Reference rs786205564(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IMPG2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.100962901C>T
CLNSRC
CLNACC RCV000171366.1,