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rs797045038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045038(-;-)
Make rs797045038(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position171448795
GeneDCAF17
is asnp
is mentioned by
dbSNPrs797045038
dbSNP (classic)rs797045038
ClinGenrs797045038
ebirs797045038
HLIrs797045038
Exacrs797045038
Gnomadrs797045038
Varsomers797045038
LitVarrs797045038
Maprs797045038
PheGenIrs797045038
Biobankrs797045038
1000 genomesrs797045038
hgdprs797045038
ensemblrs797045038
geneviewrs797045038
scholarrs797045038
googlers797045038
pharmgkbrs797045038
gwascentralrs797045038
openSNPrs797045038
23andMers797045038
SNPshotrs797045038
SNPdbers797045038
MSV3drs797045038
GWAS Ctlgrs797045038
Max Magnitude0
ClinVar
Risk rs797045038(-;-)
Alt rs797045038(-;-)
Reference Rs797045038(C;C)
Significance Pathogenic
Disease Hypogonadism not provided
Variation info
Gene DCAF17
CLNDBN Hypogonadism, diabetes mellitus, alopecia, mental retardation and electrocardiographic abnormalities not provided
Reversed 0
HGVS NC_000002.11:g.172305305delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000191077.4, RCV000278884.1,