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rs145639028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145639028(A;A)
Make rs145639028(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position6289047
GeneWFS1
is asnp
is mentioned by
dbSNPrs145639028
dbSNP (old)rs145639028
ClinGenrs145639028
ebirs145639028
HLIrs145639028
Exacrs145639028
Gnomadrs145639028
Varsomers145639028
LitVarrs145639028
Maprs145639028
PheGenIrs145639028
Biobankrs145639028
1000 genomesrs145639028
hgdprs145639028
ensemblrs145639028
gopubmedrs145639028
geneviewrs145639028
scholarrs145639028
googlers145639028
pharmgkbrs145639028
gwascentralrs145639028
openSNPrs145639028
23andMers145639028
23andMe allrs145639028
SNPshotrs145639028
SNPdbers145639028
MSV3drs145639028
GWAS Ctlgrs145639028
Max Magnitude0
ClinVar
Risk rs145639028(A;A)
Alt rs145639028(A;A)
Reference Rs145639028(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6290774G>A
CLNSRC
CLNACC RCV000413912.1,