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rs1057523792

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057523792(C;T)
Make rs1057523792(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position7752496
GeneCAMTA1
is asnp
is mentioned by
dbSNPrs1057523792
dbSNP (old)rs1057523792
ClinGenrs1057523792
ebirs1057523792
HLIrs1057523792
Exacrs1057523792
Gnomadrs1057523792
Varsomers1057523792
LitVarrs1057523792
Maprs1057523792
PheGenIrs1057523792
Biobankrs1057523792
1000 genomesrs1057523792
hgdprs1057523792
ensemblrs1057523792
gopubmedrs1057523792
geneviewrs1057523792
scholarrs1057523792
googlers1057523792
pharmgkbrs1057523792
gwascentralrs1057523792
openSNPrs1057523792
23andMers1057523792
23andMe allrs1057523792
SNPshotrs1057523792
SNPdbers1057523792
MSV3drs1057523792
GWAS Ctlgrs1057523792
Max Magnitude0
ClinVar
Risk rs1057523792(T;T)
Alt rs1057523792(T;T)
Reference Rs1057523792(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CAMTA1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.7812556C>T
CLNSRC
CLNACC RCV000439913.1,