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rs104894362

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894362(C;G)
Make rs104894362(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position25209894
GeneKRAS
is asnp
is mentioned by
dbSNPrs104894362
ebirs104894362
HLIrs104894362
Exacrs104894362
Varsomers104894362
Maprs104894362
PheGenIrs104894362
hapmaprs104894362
1000 genomesrs104894362
hgdprs104894362
ensemblrs104894362
gopubmedrs104894362
geneviewrs104894362
scholarrs104894362
googlers104894362
pharmgkbrs104894362
gwascentralrs104894362
openSNPrs104894362
23andMers104894362
23andMe allrs104894362
SNP Nexus

SNPshotrs104894362
SNPdbers104894362
MSV3drs104894362
GWAS Ctlgrs104894362
Max Magnitude0
OMIM190070
Desc
Variant0018
Relatedalso
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 RCV000013426.25, RCV000157942.1,