rs776569472

Orientation

plus

Stabilized

plus

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

Make rs776569472(-;-)

Make rs776569472(-;AA)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

165021296

Gene

SI

is a	snp
is	mentioned by
dbSNP	rs776569472
dbSNP (classic)	rs776569472
ClinGen	rs776569472
ebi	rs776569472
HLI	rs776569472
Exac	rs776569472
Gnomad	rs776569472
Varsome	rs776569472
LitVar	rs776569472
Map	rs776569472
PheGenI	rs776569472
Biobank	rs776569472
1000 genomes	rs776569472
hgdp	rs776569472
ensembl	rs776569472
geneview	rs776569472
scholar	rs776569472
google	rs776569472
pharmgkb	rs776569472
gwascentral	rs776569472
openSNP	rs776569472
23andMe	rs776569472
SNPshot	rs776569472
SNPdbe	rs776569472
MSV3d	rs776569472
GWAS Ctlg	rs776569472

Max Magnitude

0

ClinVar
Risk	rs776569472(-;-)
Alt	rs776569472(-;-)
Reference	Rs776569472(AA;AA)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SI
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.164739084_164739085delAA
CLNSRC
CLNACC	RCV000479995.1,