Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519246

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519246(-;-)
Make rs1057519246(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position94603448
GeneCASD1, SGCE
is asnp
is mentioned by
dbSNPrs1057519246
dbSNP (old)rs1057519246
ClinGenrs1057519246
ebirs1057519246
HLIrs1057519246
Exacrs1057519246
Gnomadrs1057519246
Varsomers1057519246
Maprs1057519246
PheGenIrs1057519246
Biobankrs1057519246
1000 genomesrs1057519246
hgdprs1057519246
ensemblrs1057519246
gopubmedrs1057519246
geneviewrs1057519246
scholarrs1057519246
googlers1057519246
pharmgkbrs1057519246
gwascentralrs1057519246
openSNPrs1057519246
23andMers1057519246
23andMe allrs1057519246
SNPshotrs1057519246
SNPdbers1057519246
MSV3drs1057519246
GWAS Ctlgrs1057519246
Max Magnitude0
ClinVar
Risk rs1057519246(-;-)
Alt rs1057519246(-;-)
Reference Rs1057519246(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SGCE
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.94232760delA
CLNSRC
CLNACC RCV000416161.1,