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rs757091694

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs757091694(C;C)
Make rs757091694(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position36067906
GeneWDR62
is asnp
is mentioned by
dbSNPrs757091694
dbSNP (classic)rs757091694
ClinGenrs757091694
ebirs757091694
HLIrs757091694
Exacrs757091694
Gnomadrs757091694
Varsomers757091694
LitVarrs757091694
Maprs757091694
PheGenIrs757091694
Biobankrs757091694
1000 genomesrs757091694
hgdprs757091694
ensemblrs757091694
geneviewrs757091694
scholarrs757091694
googlers757091694
pharmgkbrs757091694
gwascentralrs757091694
openSNPrs757091694
23andMers757091694
SNPshotrs757091694
SNPdbers757091694
MSV3drs757091694
GWAS Ctlgrs757091694
Max Magnitude0
ClinVar
Risk rs757091694(C;C)
Alt rs757091694(C;C)
Reference Rs757091694(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WDR62
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.36558808T>C
CLNSRC
CLNACC RCV000413566.1,