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rs786205473

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205473(C;T)
Make rs786205473(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position865122
GeneWNK1
is asnp
is mentioned by
dbSNPrs786205473
ebirs786205473
HLIrs786205473
Exacrs786205473
Varsomers786205473
Maprs786205473
PheGenIrs786205473
hapmaprs786205473
1000 genomesrs786205473
hgdprs786205473
ensemblrs786205473
gopubmedrs786205473
geneviewrs786205473
scholarrs786205473
googlers786205473
pharmgkbrs786205473
gwascentralrs786205473
openSNPrs786205473
23andMers786205473
23andMe allrs786205473
SNP Nexus

SNPshotrs786205473
SNPdbers786205473
MSV3drs786205473
GWAS Ctlgrs786205473
Max Magnitude0
ClinVar
Risk rs786205473(T;T)
Alt rs786205473(T;T)
Reference rs786205473(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WNK1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.974288C>T
CLNSRC
CLNACC RCV000171203.1,