rs121909252

Orientation

plus

Stabilized

plus

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

Make rs121909252(A;A)

Make rs121909252(A;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

110719667

Gene

ING1

is a	snp
is	mentioned by
dbSNP	rs121909252
dbSNP (classic)	rs121909252
ClinGen	rs121909252
ebi	rs121909252
HLI	rs121909252
Exac	rs121909252
Gnomad	rs121909252
Varsome	rs121909252
LitVar	rs121909252
Map	rs121909252
PheGenI	rs121909252
Biobank	rs121909252
1000 genomes	rs121909252
hgdp	rs121909252
ensembl	rs121909252
geneview	rs121909252
scholar	rs121909252
google	rs121909252
pharmgkb	rs121909252
gwascentral	rs121909252
openSNP	rs121909252
23andMe	rs121909252
SNPshot	rs121909252
SNPdbe	rs121909252
MSV3d	rs121909252
GWAS Ctlg	rs121909252

Max Magnitude

0

OMIM	601566
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909252(A;A)
Alt	rs121909252(A;A)
Reference	Rs121909252(C;C)
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.111372014C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008535.4,