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

rs104894365

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894365(A;A)
Make rs104894365(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position25245345
GeneKRAS
is asnp
is mentioned by
dbSNPrs104894365
ebirs104894365
HLIrs104894365
Exacrs104894365
Varsomers104894365
Maprs104894365
PheGenIrs104894365
hapmaprs104894365
1000 genomesrs104894365
hgdprs104894365
ensemblrs104894365
gopubmedrs104894365
geneviewrs104894365
scholarrs104894365
googlers104894365
pharmgkbrs104894365
gwascentralrs104894365
openSNPrs104894365
23andMers104894365
23andMe allrs104894365
SNP Nexus

SNPshotrs104894365
SNPdbers104894365
MSV3drs104894365
GWAS Ctlgrs104894365
Max Magnitude0
OMIM190070
Desc
Variant0012
Relatedalso
OMIM608089
Desc
Variant
Relatedalso
ClinVar
Risk rs104894365(A;A)
Alt rs104894365(A;A)
Reference rs104894365(G;G)
Significance Pathogenic
Disease Noonan syndrome 3 Endometrial carcinoma Rasopathy not provided
Variation info
Gene KRAS
CLNDBN Noonan syndrome 3 Endometrial carcinoma Rasopathy not provided
Reversed 1
HGVS NC_000012.11:g.25398279C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013420.19, RCV000119792.1, RCV000157945.1, RCV000212499.1,