rs761440783

Orientation

plus

Stabilized

plus

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

Make rs761440783(A;A)

Make rs761440783(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

61839540

Gene

FAM161A

is a	snp
is	mentioned by
dbSNP	rs761440783
dbSNP (classic)	rs761440783
ClinGen	rs761440783
ebi	rs761440783
HLI	rs761440783
Exac	rs761440783
Gnomad	rs761440783
Varsome	rs761440783
LitVar	rs761440783
Map	rs761440783
PheGenI	rs761440783
Biobank	rs761440783
1000 genomes	rs761440783
hgdp	rs761440783
ensembl	rs761440783
geneview	rs761440783
scholar	rs761440783
google	rs761440783
pharmgkb	rs761440783
gwascentral	rs761440783
openSNP	rs761440783
23andMe	rs761440783
SNPshot	rs761440783
SNPdbe	rs761440783
MSV3d	rs761440783
GWAS Ctlg	rs761440783

Max Magnitude

0

ClinVar
Risk	rs761440783(A;A) rs761440783(T;T)
Alt	rs761440783(A;A) rs761440783(T;T)
Reference	Rs761440783(C;C)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	FAM161A
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000002.11:g.62066675C>T
CLNSRC
CLNACC	RCV000225381.1,