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rs786205494

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205494(G;G)
Make rs786205494(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89210721
GeneRLBP1
is asnp
is mentioned by
dbSNPrs786205494
ebirs786205494
HLIrs786205494
Exacrs786205494
Varsomers786205494
Maprs786205494
PheGenIrs786205494
hapmaprs786205494
1000 genomesrs786205494
hgdprs786205494
ensemblrs786205494
gopubmedrs786205494
geneviewrs786205494
scholarrs786205494
googlers786205494
pharmgkbrs786205494
gwascentralrs786205494
openSNPrs786205494
23andMers786205494
23andMe allrs786205494
SNP Nexus

SNPshotrs786205494
SNPdbers786205494
MSV3drs786205494
GWAS Ctlgrs786205494
Max Magnitude0
ClinVar
Risk rs786205494(G;G)
Alt rs786205494(G;G)
Reference rs786205494(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RLBP1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89753952A>C
CLNSRC
CLNACC RCV000171241.1,