rs780389591

Orientation

plus

Stabilized

plus

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

Make rs780389591(A;A)

Make rs780389591(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

219570282

Gene	INHA, OBSL1

is a	snp
is	mentioned by
dbSNP	rs780389591
dbSNP (classic)	rs780389591
ClinGen	rs780389591
ebi	rs780389591
HLI	rs780389591
Exac	rs780389591
Gnomad	rs780389591
Varsome	rs780389591
LitVar	rs780389591
Map	rs780389591
PheGenI	rs780389591
Biobank	rs780389591
1000 genomes	rs780389591
hgdp	rs780389591
ensembl	rs780389591
geneview	rs780389591
scholar	rs780389591
google	rs780389591
pharmgkb	rs780389591
gwascentral	rs780389591
openSNP	rs780389591
23andMe	rs780389591
SNPshot	rs780389591
SNPdbe	rs780389591
MSV3d	rs780389591
GWAS Ctlg	rs780389591

Max Magnitude

0

ClinVar
Risk	rs780389591(A;A) rs780389591(T;T)
Alt	rs780389591(A;A) rs780389591(T;T)
Reference	Rs780389591(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	OBSL1 INHA
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.220435004G>T
CLNSRC
CLNACC	RCV000171333.1,