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rs143064649

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143064649(A;A)
Make rs143064649(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome4
Position6301634
GeneWFS1
is asnp
is mentioned by
dbSNPrs143064649
dbSNP (old)rs143064649
ClinGenrs143064649
ebirs143064649
HLIrs143064649
Exacrs143064649
Gnomadrs143064649
Varsomers143064649
Maprs143064649
PheGenIrs143064649
Biobankrs143064649
1000 genomesrs143064649
hgdprs143064649
ensemblrs143064649
gopubmedrs143064649
geneviewrs143064649
scholarrs143064649
googlers143064649
pharmgkbrs143064649
gwascentralrs143064649
openSNPrs143064649
23andMers143064649
23andMe allrs143064649
SNPshotrs143064649
SNPdbers143064649
MSV3drs143064649
GWAS Ctlgrs143064649
Max Magnitude0
ClinVar
Risk rs143064649(A;A)
Alt rs143064649(A;A)
Reference Rs143064649(G;G)
Significance Probable-Pathogenic
Disease WFS1-Related Spectrum Disorders
Variation info
Gene WFS1
CLNDBN WFS1-Related Spectrum Disorders
Reversed 0
HGVS NC_000004.11:g.6303361G>A
CLNSRC Illumina
CLNACC RCV000285512.1,