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rs863224865

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224865(-;A)
Make rs863224865(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position171443581
GeneDCAF17
is asnp
is mentioned by
dbSNPrs863224865
ClinGenrs863224865
ebirs863224865
HLIrs863224865
Exacrs863224865
Varsomers863224865
Maprs863224865
PheGenIrs863224865
hapmaprs863224865
1000 genomesrs863224865
hgdprs863224865
ensemblrs863224865
gopubmedrs863224865
geneviewrs863224865
scholarrs863224865
googlers863224865
pharmgkbrs863224865
gwascentralrs863224865
openSNPrs863224865
23andMers863224865
23andMe allrs863224865
SNP Nexus

SNPshotrs863224865
SNPdbers863224865
MSV3drs863224865
GWAS Ctlgrs863224865
Max Magnitude0
ClinVar
Risk rs863224865(A;A)
Alt rs863224865(A;A)
Reference Rs863224865(-;-)
Significance Pathogenic
Disease Hypogonadism
Variation info
Gene DCAF17
CLNDBN Hypogonadism, diabetes mellitus, alopecia, mental retardation and electrocardiographic abnormalities
Reversed 0
HGVS NC_000002.11:g.172300091dupA
CLNSRC
CLNACC RCV000196292.1,