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rs1045109000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position15544148
GeneCYP4F22
is asnp
is mentioned by
dbSNPrs1045109000
dbSNP (old)rs1045109000
ClinGenrs1045109000
ebirs1045109000
HLIrs1045109000
Exacrs1045109000
Gnomadrs1045109000
Varsomers1045109000
Maprs1045109000
PheGenIrs1045109000
Biobankrs1045109000
1000 genomesrs1045109000
hgdprs1045109000
ensemblrs1045109000
gopubmedrs1045109000
geneviewrs1045109000
scholarrs1045109000
googlers1045109000
pharmgkbrs1045109000
gwascentralrs1045109000
openSNPrs1045109000
23andMers1045109000
23andMe allrs1045109000
SNPshotrs1045109000
SNPdbers1045109000
MSV3drs1045109000
GWAS Ctlgrs1045109000
Max Magnitude0
ClinVar
Risk rs1045109000(G;G)
Alt rs1045109000(G;G)
Reference Rs1045109000(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.15654959A>G
CLNSRC
CLNACC RCV000493179.1,