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rs387907206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907206(A;G)
Make rs387907206(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position25225625
GeneKRAS
is asnp
is mentioned by
dbSNPrs387907206
ebirs387907206
HLIrs387907206
Exacrs387907206
Varsomers387907206
Maprs387907206
PheGenIrs387907206
hapmaprs387907206
1000 genomesrs387907206
hgdprs387907206
ensemblrs387907206
gopubmedrs387907206
geneviewrs387907206
scholarrs387907206
googlers387907206
pharmgkbrs387907206
gwascentralrs387907206
openSNPrs387907206
23andMers387907206
23andMe allrs387907206
SNP Nexus

SNPshotrs387907206
SNPdbers387907206
MSV3drs387907206
GWAS Ctlgrs387907206
Max Magnitude0
ClinVar
Risk rs387907206(G;G)
Alt rs387907206(G;G)
Reference rs387907206(A;A)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome 2
Variation info
Gene KRAS
CLNDBN Cardiofaciocutaneous syndrome 2
Reversed 1
HGVS NC_000012.11:g.25378559T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000024618.20,