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rs797044562

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044562(C;C)
Make rs797044562(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position49217759
GeneCACNA1F
is asnp
is mentioned by
dbSNPrs797044562
ebirs797044562
HLIrs797044562
Exacrs797044562
Varsomers797044562
Maprs797044562
PheGenIrs797044562
hapmaprs797044562
1000 genomesrs797044562
hgdprs797044562
ensemblrs797044562
gopubmedrs797044562
geneviewrs797044562
scholarrs797044562
googlers797044562
pharmgkbrs797044562
gwascentralrs797044562
openSNPrs797044562
23andMers797044562
23andMe allrs797044562
SNP Nexus

SNPshotrs797044562
SNPdbers797044562
MSV3drs797044562
GWAS Ctlgrs797044562
Max Magnitude0
ClinVar
Risk rs797044562(C;C)
Alt rs797044562(C;C)
Reference rs797044562(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CACNA1F
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.49074218A>G
CLNSRC
CLNACC RCV000171437.1,