rs121909250

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs121909250(C;C)

Make rs121909250(C;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

110719736

Gene

ING1

is a	snp
is	mentioned by
dbSNP	rs121909250
dbSNP (classic)	rs121909250
ClinGen	rs121909250
ebi	rs121909250
HLI	rs121909250
Exac	rs121909250
Gnomad	rs121909250
Varsome	rs121909250
LitVar	rs121909250
Map	rs121909250
PheGenI	rs121909250
Biobank	rs121909250
1000 genomes	rs121909250
hgdp	rs121909250
ensembl	rs121909250
geneview	rs121909250
scholar	rs121909250
google	rs121909250
pharmgkb	rs121909250
gwascentral	rs121909250
openSNP	rs121909250
23andMe	rs121909250
SNPshot	rs121909250
SNPdbe	rs121909250
MSV3d	rs121909250
GWAS Ctlg	rs121909250

Max Magnitude

0

OMIM	601566
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909250(C;C)
Alt	rs121909250(C;C)
Reference	Rs121909250(G;G)
Significance	Pathogenic
Disease	Squamous cell carcinoma of the head and neck
Variation	info
Gene	ING1
CLNDBN	Squamous cell carcinoma of the head and neck
Reversed	0
HGVS	NC_000013.10:g.111372083G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008533.4,