Have questions? Visit https://www.reddit.com/r/SNPedia

rs568165874

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs568165874(C;T)
Make rs568165874(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position57763738
GeneCYP27B1
is asnp
is mentioned by
dbSNPrs568165874
dbSNP (classic)rs568165874
ClinGenrs568165874
ebirs568165874
HLIrs568165874
Exacrs568165874
Gnomadrs568165874
Varsomers568165874
LitVarrs568165874
Maprs568165874
PheGenIrs568165874
Biobankrs568165874
1000 genomesrs568165874
hgdprs568165874
ensemblrs568165874
geneviewrs568165874
scholarrs568165874
googlers568165874
pharmgkbrs568165874
gwascentralrs568165874
openSNPrs568165874
23andMers568165874
23andMe allrs568165874
SNPshotrs568165874
SNPdbers568165874
MSV3drs568165874
GWAS Ctlgrs568165874
Max Magnitude0
ClinVar
Risk rs568165874(G;G) rs568165874(T;T)
Alt rs568165874(G;G) rs568165874(T;T)
Reference Rs568165874(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CYP27B1
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.58157521C>G
CLNSRC
CLNACC RCV000255484.1,