rs121913535

Orientation

minus

Stabilized

minus

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

Make rs121913535(G;T)

Make rs121913535(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

25245348

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs121913535
dbSNP (classic)	rs121913535
ClinGen	rs121913535
ebi	rs121913535
HLI	rs121913535
Exac	rs121913535
Gnomad	rs121913535
Varsome	rs121913535
LitVar	rs121913535
Map	rs121913535
PheGenI	rs121913535
Biobank	rs121913535
1000 genomes	rs121913535
hgdp	rs121913535
ensembl	rs121913535
geneview	rs121913535
scholar	rs121913535
google	rs121913535
pharmgkb	rs121913535
gwascentral	rs121913535
openSNP	rs121913535
23andMe	rs121913535
SNPshot	rs121913535
SNPdbe	rs121913535
MSV3d	rs121913535
GWAS Ctlg	rs121913535

Max Magnitude

0

OMIM	190070
Desc
Variant	0016
Related	also

ClinVar
Risk	rs121913535(A;A) rs121913535(C;C) rs121913535(T;T)
Alt	rs121913535(A;A) rs121913535(C;C) rs121913535(T;T)
Reference	Rs121913535(G;G)
Significance	Pathogenic
Disease	Non-small cell lung cancer RAS-associated autoimmune leukoproliferative disorder Colorectal Neoplasms Pilocytic astrocytoma Neoplasm of the thyroid gland
Variation	info
Gene	KRAS
CLNDBN	Non-small cell lung cancer RAS-associated autoimmune leukoproliferative disorder Colorectal Neoplasms Pilocytic astrocytoma Neoplasm of the thyroid gland
Reversed	1
HGVS	NC_000012.11:g.25398282C>A; NC_000012.11:g.25398282C>G; NC_000012.11:g.25398282C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000038268.3, RCV000144972.4, RCV000443868.1, RCV000013424.5, RCV000038267.3, RCV000426673.1, RCV000436657.1, RCV000418407.1, RCV000429548.1, RCV000436018.1,