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

rs1085307654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome19
Position15551293
GeneCYP4F22
is asnp
is mentioned by
dbSNPrs1085307654
dbSNP (classic)rs1085307654
ClinGenrs1085307654
ebirs1085307654
HLIrs1085307654
Exacrs1085307654
Gnomadrs1085307654
Varsomers1085307654
LitVarrs1085307654
Maprs1085307654
PheGenIrs1085307654
Biobankrs1085307654
1000 genomesrs1085307654
hgdprs1085307654
ensemblrs1085307654
geneviewrs1085307654
scholarrs1085307654
googlers1085307654
pharmgkbrs1085307654
gwascentralrs1085307654
openSNPrs1085307654
23andMers1085307654
23andMe allrs1085307654
SNPshotrs1085307654
SNPdbers1085307654
MSV3drs1085307654
GWAS Ctlgrs1085307654
Max Magnitude0
ClinVar
Risk rs1085307654(A;A)
Alt rs1085307654(A;A)
Reference Rs1085307654(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CYP4F22
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.15662104G>A
CLNSRC
CLNACC RCV000489832.1,