rs121912469

Orientation

minus

Stabilized

minus

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

Make rs121912469(A;T)

Make rs121912469(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

132489457

Gene

IRF1

is a	snp
is	mentioned by
dbSNP	rs121912469
dbSNP (classic)	rs121912469
ClinGen	rs121912469
ebi	rs121912469
HLI	rs121912469
Exac	rs121912469
Gnomad	rs121912469
Varsome	rs121912469
LitVar	rs121912469
Map	rs121912469
PheGenI	rs121912469
Biobank	rs121912469
1000 genomes	rs121912469
hgdp	rs121912469
ensembl	rs121912469
geneview	rs121912469
scholar	rs121912469
google	rs121912469
pharmgkb	rs121912469
gwascentral	rs121912469
openSNP	rs121912469
23andMe	rs121912469
SNPshot	rs121912469
SNPdbe	rs121912469
MSV3d	rs121912469
GWAS Ctlg	rs121912469

Max Magnitude

0

OMIM	147575
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121912469(T;T)
Alt	rs121912469(T;T)
Reference	Rs121912469(A;A)
Significance	Pathogenic
Disease	Neoplasm of stomach
Variation	info
Gene	IRF1
CLNDBN	Neoplasm of stomach
Reversed	1
HGVS	NC_000005.9:g.131825149T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015840.4,