rs779204655

Orientation

plus

Stabilized

plus

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

Make rs779204655(C;T)

Make rs779204655(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

72891406

Gene

SPR

is a	snp
is	mentioned by
dbSNP	rs779204655
dbSNP (classic)	rs779204655
ClinGen	rs779204655
ebi	rs779204655
HLI	rs779204655
Exac	rs779204655
Gnomad	rs779204655
Varsome	rs779204655
LitVar	rs779204655
Map	rs779204655
PheGenI	rs779204655
Biobank	rs779204655
1000 genomes	rs779204655
hgdp	rs779204655
ensembl	rs779204655
geneview	rs779204655
scholar	rs779204655
google	rs779204655
pharmgkb	rs779204655
gwascentral	rs779204655
openSNP	rs779204655
23andMe	rs779204655
SNPshot	rs779204655
SNPdbe	rs779204655
MSV3d	rs779204655
GWAS Ctlg	rs779204655

Max Magnitude

0

ClinVar
Risk	rs779204655(T;T)
Alt	rs779204655(T;T)
Reference	Rs779204655(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SPR
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.73118535C>T
CLNSRC
CLNACC	RCV000224347.1,