rs780535026

Orientation

plus

Stabilized

plus

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

Make rs780535026(-;-)

Make rs780535026(-;AT)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

165017807

Gene

SI

is a	snp
is	mentioned by
dbSNP	rs780535026
dbSNP (classic)	rs780535026
ClinGen	rs780535026
ebi	rs780535026
HLI	rs780535026
Exac	rs780535026
Gnomad	rs780535026
Varsome	rs780535026
LitVar	rs780535026
Map	rs780535026
PheGenI	rs780535026
Biobank	rs780535026
1000 genomes	rs780535026
hgdp	rs780535026
ensembl	rs780535026
geneview	rs780535026
scholar	rs780535026
google	rs780535026
pharmgkb	rs780535026
gwascentral	rs780535026
openSNP	rs780535026
23andMe	rs780535026
SNPshot	rs780535026
SNPdbe	rs780535026
MSV3d	rs780535026
GWAS Ctlg	rs780535026

Max Magnitude

0

ClinVar
Risk	rs780535026(-;-)
Alt	rs780535026(-;-)
Reference	Rs780535026(AT;AT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SI
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.164735595_164735596delAT
CLNSRC
CLNACC	RCV000482732.1,