rs786205546

Orientation

minus

Stabilized

minus

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

Make rs786205546(C;C)

Make rs786205546(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

208124230

Gene	CRYGD, LOC100507443

is a	snp
is	mentioned by
dbSNP	rs786205546
dbSNP (classic)	rs786205546
ClinGen	rs786205546
ebi	rs786205546
HLI	rs786205546
Exac	rs786205546
Gnomad	rs786205546
Varsome	rs786205546
LitVar	rs786205546
Map	rs786205546
PheGenI	rs786205546
Biobank	rs786205546
1000 genomes	rs786205546
hgdp	rs786205546
ensembl	rs786205546
geneview	rs786205546
scholar	rs786205546
google	rs786205546
pharmgkb	rs786205546
gwascentral	rs786205546
openSNP	rs786205546
23andMe	rs786205546
SNPshot	rs786205546
SNPdbe	rs786205546
MSV3d	rs786205546
GWAS Ctlg	rs786205546

Max Magnitude

0

ClinVar
Risk	rs786205546(C;C)
Alt	rs786205546(C;C)
Reference	Rs786205546(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CRYGD LOC100507443
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.208988954A>G
CLNSRC
CLNACC	RCV000171329.1,