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rs745368359

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745368359(C;T)
Make rs745368359(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position15544227
GeneCYP4F22
is asnp
is mentioned by
dbSNPrs745368359
dbSNP (classic)rs745368359
ClinGenrs745368359
ebirs745368359
HLIrs745368359
Exacrs745368359
Gnomadrs745368359
Varsomers745368359
LitVarrs745368359
Maprs745368359
PheGenIrs745368359
Biobankrs745368359
1000 genomesrs745368359
hgdprs745368359
ensemblrs745368359
geneviewrs745368359
scholarrs745368359
googlers745368359
pharmgkbrs745368359
gwascentralrs745368359
openSNPrs745368359
23andMers745368359
SNPshotrs745368359
SNPdbers745368359
MSV3drs745368359
GWAS Ctlgrs745368359
Max Magnitude0
ClinVar
Risk rs745368359(T;T)
Alt rs745368359(T;T)
Reference Rs745368359(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CYP4F22
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.15655038C>T
CLNSRC
CLNACC RCV000426277.1,