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rs1064797339

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position94629758
GeneCASD1, SGCE
is asnp
is mentioned by
dbSNPrs1064797339
dbSNP (classic)rs1064797339
ClinGenrs1064797339
ebirs1064797339
HLIrs1064797339
Exacrs1064797339
Gnomadrs1064797339
Varsomers1064797339
LitVarrs1064797339
Maprs1064797339
PheGenIrs1064797339
Biobankrs1064797339
1000 genomesrs1064797339
hgdprs1064797339
ensemblrs1064797339
geneviewrs1064797339
scholarrs1064797339
googlers1064797339
pharmgkbrs1064797339
gwascentralrs1064797339
openSNPrs1064797339
23andMers1064797339
23andMe allrs1064797339
SNPshotrs1064797339
SNPdbers1064797339
MSV3drs1064797339
GWAS Ctlgrs1064797339
Max Magnitude0
ClinVar
Risk rs1064797339(T;T)
Alt rs1064797339(T;T)
Reference Rs1064797339(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SGCE
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.94259070C>A
CLNSRC
CLNACC RCV000487622.1,