rs62637337

Orientation

plus

Stabilized

plus

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

Make rs62637337(C;C)

Make rs62637337(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

11

Position

61956999

Gene	BEST1, LOC107984334

is a	snp
is	mentioned by
dbSNP	rs62637337
dbSNP (classic)	rs62637337
ClinGen	rs62637337
ebi	rs62637337
HLI	rs62637337
Exac	rs62637337
Gnomad	rs62637337
Varsome	rs62637337
LitVar	rs62637337
Map	rs62637337
PheGenI	rs62637337
Biobank	rs62637337
1000 genomes	rs62637337
hgdp	rs62637337
ensembl	rs62637337
geneview	rs62637337
scholar	rs62637337
google	rs62637337
pharmgkb	rs62637337
gwascentral	rs62637337
openSNP	rs62637337
23andMe	rs62637337
SNPshot	rs62637337
SNPdbe	rs62637337
MSV3d	rs62637337
GWAS Ctlg	rs62637337

Max Magnitude

0

ClinVar
Risk	rs62637337(A;A) rs62637337(C;C) rs62637337(T;T)
Alt	rs62637337(A;A) rs62637337(C;C) rs62637337(T;T)
Reference	Rs62637337(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	BEST1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.61724471G>A; NC_000011.9:g.61724471G>C
CLNSRC
CLNACC	RCV000255249.1, RCV000086146.1,