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rs727503845

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503845(C;T)
Make rs727503845(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position47227098
GeneCDK16
is asnp
is mentioned by
dbSNPrs727503845
ebirs727503845
HLIrs727503845
Exacrs727503845
Varsomers727503845
Maprs727503845
PheGenIrs727503845
hapmaprs727503845
1000 genomesrs727503845
hgdprs727503845
ensemblrs727503845
gopubmedrs727503845
geneviewrs727503845
scholarrs727503845
googlers727503845
pharmgkbrs727503845
gwascentralrs727503845
openSNPrs727503845
23andMers727503845
23andMe allrs727503845
SNP Nexus

SNPshotrs727503845
SNPdbers727503845
MSV3drs727503845
GWAS Ctlgrs727503845
Max Magnitude0
ClinVar
Risk rs727503845(T;T)
Alt rs727503845(T;T)
Reference rs727503845(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CDK16
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.47086497C>T
CLNSRC
CLNACC RCV000152957.3,