rs779803851

Orientation

plus

Stabilized

plus

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

Make rs779803851(A;A)

Make rs779803851(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

3

Position

164987225

Gene

SI

is a	snp
is	mentioned by
dbSNP	rs779803851
dbSNP (classic)	rs779803851
ClinGen	rs779803851
ebi	rs779803851
HLI	rs779803851
Exac	rs779803851
Gnomad	rs779803851
Varsome	rs779803851
LitVar	rs779803851
Map	rs779803851
PheGenI	rs779803851
Biobank	rs779803851
1000 genomes	rs779803851
hgdp	rs779803851
ensembl	rs779803851
geneview	rs779803851
scholar	rs779803851
google	rs779803851
pharmgkb	rs779803851
gwascentral	rs779803851
openSNP	rs779803851
23andMe	rs779803851
SNPshot	rs779803851
SNPdbe	rs779803851
MSV3d	rs779803851
GWAS Ctlg	rs779803851

Max Magnitude

0

ClinVar
Risk	rs779803851(A;A)
Alt	rs779803851(A;A)
Reference	Rs779803851(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SI
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.164705013G>A
CLNSRC
CLNACC	RCV000255674.1,