rs786205664

Orientation

minus

Stabilized

minus

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

Make rs786205664(A;T)

Make rs786205664(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

111120671

Gene

DRAM2

is a	snp
is	mentioned by
dbSNP	rs786205664
dbSNP (classic)	rs786205664
ClinGen	rs786205664
ebi	rs786205664
HLI	rs786205664
Exac	rs786205664
Gnomad	rs786205664
Varsome	rs786205664
LitVar	rs786205664
Map	rs786205664
PheGenI	rs786205664
Biobank	rs786205664
1000 genomes	rs786205664
hgdp	rs786205664
ensembl	rs786205664
geneview	rs786205664
scholar	rs786205664
google	rs786205664
pharmgkb	rs786205664
gwascentral	rs786205664
openSNP	rs786205664
23andMe	rs786205664
SNPshot	rs786205664
SNPdbe	rs786205664
MSV3d	rs786205664
GWAS Ctlg	rs786205664

Max Magnitude

0

ClinVar
Risk	rs786205664(T;T)
Alt	rs786205664(T;T)
Reference	Rs786205664(A;A)
Significance	Pathogenic
Disease	Retinal dystrophy Cone-rod dystrophy 21
Variation	info
Gene	DRAM2
CLNDBN	Retinal dystrophy Cone-rod dystrophy 21
Reversed	1
HGVS	NC_000001.10:g.111663293T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000172836.1, RCV000186605.2,