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rs796065318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796065318(-;GC)
Make rs796065318(GC;GC)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position50170664
GeneSGCA
is asnp
is mentioned by
dbSNPrs796065318
ClinGenrs796065318
ebirs796065318
HLIrs796065318
Exacrs796065318
Varsomers796065318
Maprs796065318
PheGenIrs796065318
hapmaprs796065318
1000 genomesrs796065318
hgdprs796065318
ensemblrs796065318
gopubmedrs796065318
geneviewrs796065318
scholarrs796065318
googlers796065318
pharmgkbrs796065318
gwascentralrs796065318
openSNPrs796065318
23andMers796065318
23andMe allrs796065318
SNP Nexus

SNPshotrs796065318
SNPdbers796065318
MSV3drs796065318
GWAS Ctlgrs796065318
Max Magnitude0
ClinVar
Risk rs796065318(CG;CG)
Alt rs796065318(CG;CG)
Reference Rs796065318(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SGCA
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.48248025_48248026insGC
CLNSRC
CLNACC RCV000171485.1,