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rs1057523895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057523895(A;C)
Make rs1057523895(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position49213904
GeneCACNA1F
is asnp
is mentioned by
dbSNPrs1057523895
dbSNP (classic)rs1057523895
ClinGenrs1057523895
ebirs1057523895
HLIrs1057523895
Exacrs1057523895
Gnomadrs1057523895
Varsomers1057523895
LitVarrs1057523895
Maprs1057523895
PheGenIrs1057523895
Biobankrs1057523895
1000 genomesrs1057523895
hgdprs1057523895
ensemblrs1057523895
geneviewrs1057523895
scholarrs1057523895
googlers1057523895
pharmgkbrs1057523895
gwascentralrs1057523895
openSNPrs1057523895
23andMers1057523895
SNPshotrs1057523895
SNPdbers1057523895
MSV3drs1057523895
GWAS Ctlgrs1057523895
Max Magnitude0
ClinVar
Risk rs1057523895(C;C)
Alt rs1057523895(C;C)
Reference Rs1057523895(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CACNA1F
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.49070364T>G
CLNSRC
CLNACC RCV000436235.1,