rs761628767

Orientation

plus

Stabilized

plus

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

Make rs761628767(A;A)

Make rs761628767(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

71813567

Gene

NR2E3

is a	snp
is	mentioned by
dbSNP	rs761628767
dbSNP (classic)	rs761628767
ClinGen	rs761628767
ebi	rs761628767
HLI	rs761628767
Exac	rs761628767
Gnomad	rs761628767
Varsome	rs761628767
LitVar	rs761628767
Map	rs761628767
PheGenI	rs761628767
Biobank	rs761628767
1000 genomes	rs761628767
hgdp	rs761628767
ensembl	rs761628767
geneview	rs761628767
scholar	rs761628767
google	rs761628767
pharmgkb	rs761628767
gwascentral	rs761628767
openSNP	rs761628767
23andMe	rs761628767
SNPshot	rs761628767
SNPdbe	rs761628767
MSV3d	rs761628767
GWAS Ctlg	rs761628767

Max Magnitude

0

ClinVar
Risk	rs761628767(A;A) rs761628767(T;T)
Alt	rs761628767(A;A) rs761628767(T;T)
Reference	Rs761628767(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NR2E3
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.72105907G>T
CLNSRC
CLNACC	RCV000171239.1,