rs17851045

Orientation

minus

Stabilized

minus

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

Make rs17851045(A;C)

Make rs17851045(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

25227341

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs17851045
dbSNP (classic)	rs17851045
ClinGen	rs17851045
ebi	rs17851045
HLI	rs17851045
Exac	rs17851045
Gnomad	rs17851045
Varsome	rs17851045
LitVar	rs17851045
Map	rs17851045
PheGenI	rs17851045
Biobank	rs17851045
1000 genomes	rs17851045
hgdp	rs17851045
ensembl	rs17851045
geneview	rs17851045
scholar	rs17851045
google	rs17851045
pharmgkb	rs17851045
gwascentral	rs17851045
openSNP	rs17851045
23andMe	rs17851045
SNPshot	rs17851045
SNPdbe	rs17851045
MSV3d	rs17851045
GWAS Ctlg	rs17851045

Max Magnitude

0

ClinVar
Risk	rs17851045(C;C) rs17851045(T;T)
Alt	rs17851045(C;C) rs17851045(T;T)
Reference	Rs17851045(A;A)
Significance	Pathogenic
Disease	Non-small cell lung cancer Colorectal Neoplasms Adenocarcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of lung Neoplasm of the thyroid gland Multiple myeloma Malignant neoplasm of body of uterus Chronic lymphocytic leukemia Hepatocellular carcinoma Acute myeloid leukemia Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Pancreatic adenocarcinoma
Variation	info
Gene	KRAS
CLNDBN	Non-small cell lung cancer Colorectal Neoplasms Adenocarcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of lung Neoplasm of the thyroid gland Multiple myeloma Malignant neoplasm of body of uterus Chronic lymphocytic leukemia Hepatocellular carcinoma Acute myeloid leukemia Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Pancreatic adenocarcinoma
Reversed	1
HGVS	NC_000012.11:g.25380275T>A; NC_000012.11:g.25380275T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000038259.3, RCV000417543.1, RCV000420404.1, RCV000421965.1, RCV000423293.1, RCV000423952.1, RCV000429878.1, RCV000430651.1, RCV000433108.1, RCV000433564.1, RCV000435442.1, RCV000440092.1, RCV000441804.1, RCV000445124.1, RCV000154530.3, RCV000424748.1, RCV000444370.1,