rs137853297

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;T)	6.8	Retinoblastoma (predicted)
(T;T)	0	common in clinvar

Make rs137853297(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

48456207

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs137853297
dbSNP (classic)	rs137853297
ClinGen	rs137853297
ebi	rs137853297
HLI	rs137853297
Exac	rs137853297
Gnomad	rs137853297
Varsome	rs137853297
LitVar	rs137853297
Map	rs137853297
PheGenI	rs137853297
Biobank	rs137853297
1000 genomes	rs137853297
hgdp	rs137853297
ensembl	rs137853297
geneview	rs137853297
scholar	rs137853297
google	rs137853297
pharmgkb	rs137853297
gwascentral	rs137853297
openSNP	rs137853297
23andMe	rs137853297
SNPshot	rs137853297
SNPdbe	rs137853297
MSV3d	rs137853297
GWAS Ctlg	rs137853297

Max Magnitude

6.8

OMIM	180200
Desc
Variant	0026
Related	also

ClinVar
Risk	rs137853297(A;A)
Alt	rs137853297(A;A)
Reference	Rs137853297(T;T)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.49030343T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013970.2,