Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057524638

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524638(C;T)
Make rs1057524638(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position1726523
GeneWDR81
is asnp
is mentioned by
dbSNPrs1057524638
dbSNP (old)rs1057524638
ClinGenrs1057524638
ebirs1057524638
HLIrs1057524638
Exacrs1057524638
Gnomadrs1057524638
Varsomers1057524638
Maprs1057524638
PheGenIrs1057524638
Biobankrs1057524638
1000 genomesrs1057524638
hgdprs1057524638
ensemblrs1057524638
gopubmedrs1057524638
geneviewrs1057524638
scholarrs1057524638
googlers1057524638
pharmgkbrs1057524638
gwascentralrs1057524638
openSNPrs1057524638
23andMers1057524638
23andMe allrs1057524638
SNPshotrs1057524638
SNPdbers1057524638
MSV3drs1057524638
GWAS Ctlgrs1057524638
Max Magnitude0
ClinVar
Risk rs1057524638(T;T)
Alt rs1057524638(T;T)
Reference Rs1057524638(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene WDR81
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.1629817C>T
CLNSRC
CLNACC RCV000426986.1,