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rs1057517990

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517990(G;T)
Make rs1057517990(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position94629718
GeneCASD1, SGCE
is asnp
is mentioned by
dbSNPrs1057517990
dbSNP (old)rs1057517990
ClinGenrs1057517990
ebirs1057517990
HLIrs1057517990
Exacrs1057517990
Gnomadrs1057517990
Varsomers1057517990
LitVarrs1057517990
Maprs1057517990
PheGenIrs1057517990
Biobankrs1057517990
1000 genomesrs1057517990
hgdprs1057517990
ensemblrs1057517990
gopubmedrs1057517990
geneviewrs1057517990
scholarrs1057517990
googlers1057517990
pharmgkbrs1057517990
gwascentralrs1057517990
openSNPrs1057517990
23andMers1057517990
23andMe allrs1057517990
SNPshotrs1057517990
SNPdbers1057517990
MSV3drs1057517990
GWAS Ctlgrs1057517990
Max Magnitude0
ClinVar
Risk rs1057517990(T;T)
Alt rs1057517990(T;T)
Reference Rs1057517990(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SGCE
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.94259030C>A
CLNSRC
CLNACC RCV000412835.1,