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rs786205510

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205510(C;T)
Make rs786205510(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position82619074
GeneWDR45B
is asnp
is mentioned by
dbSNPrs786205510
ebirs786205510
HLIrs786205510
Exacrs786205510
Varsomers786205510
Maprs786205510
PheGenIrs786205510
hapmaprs786205510
1000 genomesrs786205510
hgdprs786205510
ensemblrs786205510
gopubmedrs786205510
geneviewrs786205510
scholarrs786205510
googlers786205510
pharmgkbrs786205510
gwascentralrs786205510
openSNPrs786205510
23andMers786205510
23andMe allrs786205510
SNP Nexus

SNPshotrs786205510
SNPdbers786205510
MSV3drs786205510
GWAS Ctlgrs786205510
Max Magnitude0
ClinVar
Risk rs786205510(T;T)
Alt rs786205510(T;T)
Reference rs786205510(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WDR45B
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.80576950G>A
CLNSRC
CLNACC RCV000171267.1,