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rs387907205

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907205(C;C)
Make rs387907205(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25227313
GeneKRAS
is asnp
is mentioned by
dbSNPrs387907205
ebirs387907205
HLIrs387907205
Exacrs387907205
Varsomers387907205
Maprs387907205
PheGenIrs387907205
hapmaprs387907205
1000 genomesrs387907205
hgdprs387907205
ensemblrs387907205
gopubmedrs387907205
geneviewrs387907205
scholarrs387907205
googlers387907205
pharmgkbrs387907205
gwascentralrs387907205
openSNPrs387907205
23andMers387907205
23andMe allrs387907205
SNP Nexus

SNPshotrs387907205
SNPdbers387907205
MSV3drs387907205
GWAS Ctlgrs387907205
Max Magnitude0
ClinVar
Risk rs387907205(C,G;C,G)
Alt rs387907205(C,G;C,G)
Reference rs387907205(T;T)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome 1 Cardiofaciocutaneous syndrome 2
Variation info
Gene KRAS
CLNDBN Cardiofaciocutaneous syndrome 1 Cardiofaciocutaneous syndrome 2
Reversed 1
HGVS NC_000012.11:g.25380247A>C; NC_000012.11:g.25380247A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000221667.1, RCV000024617.21,