Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894359

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894359(C;C)
Make rs104894359(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position25227346
GeneKRAS
is asnp
is mentioned by
dbSNPrs104894359
ebirs104894359
HLIrs104894359
Exacrs104894359
Varsomers104894359
Maprs104894359
PheGenIrs104894359
hapmaprs104894359
1000 genomesrs104894359
hgdprs104894359
ensemblrs104894359
gopubmedrs104894359
geneviewrs104894359
scholarrs104894359
googlers104894359
pharmgkbrs104894359
gwascentralrs104894359
openSNPrs104894359
23andMers104894359
23andMe allrs104894359
SNP Nexus

SNPshotrs104894359
SNPdbers104894359
MSV3drs104894359
GWAS Ctlgrs104894359
Max Magnitude0
OMIM190070
Desc
Variant0009
Relatedalso
OMIM190070
Desc
Variant0020
Relatedalso
ClinVar
Risk rs104894359(A,C;A,C)
Alt rs104894359(A,C;A,C)
Reference rs104894359(G;G)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome 2 Rasopathy Noonan syndrome 3 not provided
Variation info
Gene KRAS
CLNDBN Cardiofaciocutaneous syndrome 2 Rasopathy Noonan syndrome 3 not provided
Reversed 1
HGVS NC_000012.11:g.25380280C>G; NC_000012.11:g.25380280C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013416.22, RCV000157935.2, RCV000013428.22, RCV000157934.2,