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rs201494527

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201494527(-;-)
Make rs201494527(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position171448667
GeneDCAF17
is asnp
is mentioned by
dbSNPrs201494527
ebirs201494527
HLIrs201494527
Exacrs201494527
Varsomers201494527
Maprs201494527
PheGenIrs201494527
hapmaprs201494527
1000 genomesrs201494527
hgdprs201494527
ensemblrs201494527
gopubmedrs201494527
geneviewrs201494527
scholarrs201494527
googlers201494527
pharmgkbrs201494527
gwascentralrs201494527
openSNPrs201494527
23andMers201494527
23andMe allrs201494527
SNP Nexus

SNPshotrs201494527
SNPdbers201494527
MSV3drs201494527
GWAS Ctlgrs201494527
Max Magnitude0
ClinVar
Risk rs201494527(;)
Alt rs201494527(;)
Reference rs201494527(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DCAF17
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.172305177delC
CLNSRC
CLNACC RCV000171501.1,