rs104894367

Orientation

minus

Stabilized

minus

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

Make rs104894367(G;G)

Make rs104894367(G;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

25209907

Gene

KRAS

is a	snp
is	mentioned by
dbSNP	rs104894367
dbSNP (classic)	rs104894367
ClinGen	rs104894367
ebi	rs104894367
HLI	rs104894367
Exac	rs104894367
Gnomad	rs104894367
Varsome	rs104894367
LitVar	rs104894367
Map	rs104894367
PheGenI	rs104894367
Biobank	rs104894367
1000 genomes	rs104894367
hgdp	rs104894367
ensembl	rs104894367
geneview	rs104894367
scholar	rs104894367
google	rs104894367
pharmgkb	rs104894367
gwascentral	rs104894367
openSNP	rs104894367
23andMe	rs104894367
SNPshot	rs104894367
SNPdbe	rs104894367
MSV3d	rs104894367
GWAS Ctlg	rs104894367

Max Magnitude

0

OMIM	190070
Desc
Variant	0014
Related	also

ClinVar
Risk	rs104894367(G;G)
Alt	rs104894367(G;G)
Reference	Rs104894367(T;T)
Significance	Pathogenic
Disease	Noonan syndrome 3
Variation	info
Gene	KRAS
CLNDBN	Noonan syndrome 3
Reversed	1
HGVS	NC_000012.11:g.25362841A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013422.21,