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rs138447882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138447882(C;T)
Make rs138447882(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position49215380
GeneCACNA1F
is asnp
is mentioned by
dbSNPrs138447882
dbSNP (old)rs138447882
ClinGenrs138447882
ebirs138447882
HLIrs138447882
Exacrs138447882
Gnomadrs138447882
Varsomers138447882
Maprs138447882
PheGenIrs138447882
Biobankrs138447882
1000 genomesrs138447882
hgdprs138447882
ensemblrs138447882
gopubmedrs138447882
geneviewrs138447882
scholarrs138447882
googlers138447882
pharmgkbrs138447882
gwascentralrs138447882
openSNPrs138447882
23andMers138447882
23andMe allrs138447882
SNPshotrs138447882
SNPdbers138447882
MSV3drs138447882
GWAS Ctlgrs138447882
Max Magnitude0
ClinVar
Risk rs138447882(A;A) rs138447882(T;T)
Alt rs138447882(A;A) rs138447882(T;T)
Reference Rs138447882(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CACNA1F
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.49071840C>A
CLNSRC
CLNACC RCV000413471.1,