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rs781923569

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781923569(C;T)
Make rs781923569(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position49231744
GeneCACNA1F
is asnp
is mentioned by
dbSNPrs781923569
ebirs781923569
HLIrs781923569
Exacrs781923569
Varsomers781923569
Maprs781923569
PheGenIrs781923569
hapmaprs781923569
1000 genomesrs781923569
hgdprs781923569
ensemblrs781923569
gopubmedrs781923569
geneviewrs781923569
scholarrs781923569
googlers781923569
pharmgkbrs781923569
gwascentralrs781923569
openSNPrs781923569
23andMers781923569
23andMe allrs781923569
SNP Nexus

SNPshotrs781923569
SNPdbers781923569
MSV3drs781923569
GWAS Ctlgrs781923569
Max Magnitude0
ClinVar
Risk rs781923569(T;T)
Alt rs781923569(T;T)
Reference rs781923569(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CACNA1F
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.49088206C>T
CLNSRC
CLNACC RCV000171438.1,