rs104894362

Orientation

minus

Stabilized

minus

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

Make rs104894362(C;G)

Make rs104894362(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

25209894

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs104894362
dbSNP (classic)	rs104894362
ClinGen	rs104894362
ebi	rs104894362
HLI	rs104894362
Exac	rs104894362
Gnomad	rs104894362
Varsome	rs104894362
LitVar	rs104894362
Map	rs104894362
PheGenI	rs104894362
Biobank	rs104894362
1000 genomes	rs104894362
hgdp	rs104894362
ensembl	rs104894362
geneview	rs104894362
scholar	rs104894362
google	rs104894362
pharmgkb	rs104894362
gwascentral	rs104894362
openSNP	rs104894362
23andMe	rs104894362
SNPshot	rs104894362
SNPdbe	rs104894362
MSV3d	rs104894362
GWAS Ctlg	rs104894362

Max Magnitude

0

OMIM	190070
Desc
Variant	0018
Related	also

ClinVar
Risk	rs104894362(G;G)
Alt	rs104894362(G;G)
Reference	Rs104894362(C;C)
Significance	Pathogenic
Disease	Cardiofaciocutaneous syndrome 2 not provided
Variation	info
Gene	KRAS
CLNDBN	Cardiofaciocutaneous syndrome 2 not provided
Reversed	1
HGVS	NC_000012.11:g.25362828G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013426.26, RCV000157942.1,