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rs770279237

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770279237(C;T)
Make rs770279237(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position1728245
GeneWDR81
is asnp
is mentioned by
dbSNPrs770279237
ebirs770279237
HLIrs770279237
Exacrs770279237
Varsomers770279237
Maprs770279237
PheGenIrs770279237
hapmaprs770279237
1000 genomesrs770279237
hgdprs770279237
ensemblrs770279237
gopubmedrs770279237
geneviewrs770279237
scholarrs770279237
googlers770279237
pharmgkbrs770279237
gwascentralrs770279237
openSNPrs770279237
23andMers770279237
23andMe allrs770279237
SNP Nexus

SNPshotrs770279237
SNPdbers770279237
MSV3drs770279237
GWAS Ctlgrs770279237
Max Magnitude0
ClinVar
Risk rs770279237(T;T)
Alt rs770279237(T;T)
Reference rs770279237(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WDR81
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.1631539C>T
CLNSRC
CLNACC RCV000171482.1,