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rs104894367

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894367(G;G)
Make rs104894367(G;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25209907
GeneKRAS
is asnp
is mentioned by
dbSNPrs104894367
ebirs104894367
HLIrs104894367
Exacrs104894367
Varsomers104894367
Maprs104894367
PheGenIrs104894367
hapmaprs104894367
1000 genomesrs104894367
hgdprs104894367
ensemblrs104894367
gopubmedrs104894367
geneviewrs104894367
scholarrs104894367
googlers104894367
pharmgkbrs104894367
gwascentralrs104894367
openSNPrs104894367
23andMers104894367
23andMe allrs104894367
SNP Nexus

SNPshotrs104894367
SNPdbers104894367
MSV3drs104894367
GWAS Ctlgrs104894367
Max Magnitude0
OMIM190070
Desc
Variant0014
Relatedalso
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 RCV000013422.20,