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rs786205465

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205465(G;T)
Make rs786205465(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position99818791
GeneABCC2
is asnp
is mentioned by
dbSNPrs786205465
ebirs786205465
HLIrs786205465
Exacrs786205465
Varsomers786205465
Maprs786205465
PheGenIrs786205465
hapmaprs786205465
1000 genomesrs786205465
hgdprs786205465
ensemblrs786205465
gopubmedrs786205465
geneviewrs786205465
scholarrs786205465
googlers786205465
pharmgkbrs786205465
gwascentralrs786205465
openSNPrs786205465
23andMers786205465
23andMe allrs786205465
SNP Nexus

SNPshotrs786205465
SNPdbers786205465
MSV3drs786205465
GWAS Ctlgrs786205465
Max Magnitude0
ClinVar
Risk rs786205465(T;T)
Alt rs786205465(T;T)
Reference rs786205465(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.101578548G>T
CLNSRC
CLNACC RCV000171189.1,