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rs786205496

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205496(A;A)
Make rs786205496(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position8768866
GeneABAT
is asnp
is mentioned by
dbSNPrs786205496
ebirs786205496
HLIrs786205496
Exacrs786205496
Varsomers786205496
Maprs786205496
PheGenIrs786205496
hapmaprs786205496
1000 genomesrs786205496
hgdprs786205496
ensemblrs786205496
gopubmedrs786205496
geneviewrs786205496
scholarrs786205496
googlers786205496
pharmgkbrs786205496
gwascentralrs786205496
openSNPrs786205496
23andMers786205496
23andMe allrs786205496
SNP Nexus

SNPshotrs786205496
SNPdbers786205496
MSV3drs786205496
GWAS Ctlgrs786205496
Max Magnitude0
ClinVar
Risk rs786205496(A;A)
Alt rs786205496(A;A)
Reference rs786205496(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABAT
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.8862723G>A
CLNSRC
CLNACC RCV000171244.1,