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rs1064793570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position50168379
GeneLOC105371818, SGCA
is asnp
is mentioned by
dbSNPrs1064793570
dbSNP (classic)rs1064793570
ClinGenrs1064793570
ebirs1064793570
HLIrs1064793570
Exacrs1064793570
Gnomadrs1064793570
Varsomers1064793570
LitVarrs1064793570
Maprs1064793570
PheGenIrs1064793570
Biobankrs1064793570
1000 genomesrs1064793570
hgdprs1064793570
ensemblrs1064793570
geneviewrs1064793570
scholarrs1064793570
googlers1064793570
pharmgkbrs1064793570
gwascentralrs1064793570
openSNPrs1064793570
23andMers1064793570
SNPshotrs1064793570
SNPdbers1064793570
MSV3drs1064793570
GWAS Ctlgrs1064793570
Max Magnitude0
ClinVar
Risk rs1064793570(-;-)
Alt rs1064793570(-;-)
Reference Rs1064793570(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SGCA
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.48245740delC
CLNSRC
CLNACC RCV000481165.1,