rs121909251

Orientation

plus

Stabilized

plus

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

Make rs121909251(A;G)

Make rs121909251(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

110719739

Gene

ING1

is a	snp
is	mentioned by
dbSNP	rs121909251
dbSNP (classic)	rs121909251
ClinGen	rs121909251
ebi	rs121909251
HLI	rs121909251
Exac	rs121909251
Gnomad	rs121909251
Varsome	rs121909251
LitVar	rs121909251
Map	rs121909251
PheGenI	rs121909251
Biobank	rs121909251
1000 genomes	rs121909251
hgdp	rs121909251
ensembl	rs121909251
geneview	rs121909251
scholar	rs121909251
google	rs121909251
pharmgkb	rs121909251
gwascentral	rs121909251
openSNP	rs121909251
23andMe	rs121909251
SNPshot	rs121909251
SNPdbe	rs121909251
MSV3d	rs121909251
GWAS Ctlg	rs121909251

Max Magnitude

0

OMIM	601566
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909251(G;G)
Alt	rs121909251(G;G)
Reference	Rs121909251(A;A)
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.111372086A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008534.4,