rs796065318

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs796065318(-;GC)

Make rs796065318(GC;GC)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

50170664

Gene

SGCA

is a	snp
is	mentioned by
dbSNP	rs796065318
dbSNP (classic)	rs796065318
ClinGen	rs796065318
ebi	rs796065318
HLI	rs796065318
Exac	rs796065318
Gnomad	rs796065318
Varsome	rs796065318
LitVar	rs796065318
Map	rs796065318
PheGenI	rs796065318
Biobank	rs796065318
1000 genomes	rs796065318
hgdp	rs796065318
ensembl	rs796065318
geneview	rs796065318
scholar	rs796065318
google	rs796065318
pharmgkb	rs796065318
gwascentral	rs796065318
openSNP	rs796065318
23andMe	rs796065318
SNPshot	rs796065318
SNPdbe	rs796065318
MSV3d	rs796065318
GWAS Ctlg	rs796065318

Max Magnitude

0

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,