rs1057519958

Orientation

plus

Stabilized

plus

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

Make rs1057519958(C;T)

Make rs1057519958(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

134436505

Gene

RXRA

is a	snp
is	mentioned by
dbSNP	rs1057519958
dbSNP (classic)	rs1057519958
ClinGen	rs1057519958
ebi	rs1057519958
HLI	rs1057519958
Exac	rs1057519958
Gnomad	rs1057519958
Varsome	rs1057519958
LitVar	rs1057519958
Map	rs1057519958
PheGenI	rs1057519958
Biobank	rs1057519958
1000 genomes	rs1057519958
hgdp	rs1057519958
ensembl	rs1057519958
geneview	rs1057519958
scholar	rs1057519958
google	rs1057519958
pharmgkb	rs1057519958
gwascentral	rs1057519958
openSNP	rs1057519958
23andMe	rs1057519958
SNPshot	rs1057519958
SNPdbe	rs1057519958
MSV3d	rs1057519958
GWAS Ctlg	rs1057519958

Max Magnitude

0

ClinVar
Risk	rs1057519958(A;A) rs1057519958(T;T)
Alt	rs1057519958(A;A) rs1057519958(T;T)
Reference	Rs1057519958(C;C)
Significance	Probable-Pathogenic
Disease	Pancreatic adenocarcinoma Transitional cell carcinoma of the bladder Hepatocellular carcinoma
Variation	info
Gene	RXRA
CLNDBN	Pancreatic adenocarcinoma Transitional cell carcinoma of the bladder Hepatocellular carcinoma
Reversed	0
HGVS	NC_000009.11:g.137328351C>A; NC_000009.11:g.137328351C>T
CLNSRC
CLNACC	RCV000419019.1, RCV000429414.1, RCV000435929.1, RCV000419754.1, RCV000425675.1, RCV000437431.1,