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rs869025608

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025608(G;T)
Make rs869025608(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position66435117
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs869025608
ebirs869025608
HLIrs869025608
Exacrs869025608
Varsomers869025608
Maprs869025608
PheGenIrs869025608
hapmaprs869025608
1000 genomesrs869025608
hgdprs869025608
ensemblrs869025608
gopubmedrs869025608
geneviewrs869025608
scholarrs869025608
googlers869025608
pharmgkbrs869025608
gwascentralrs869025608
openSNPrs869025608
23andMers869025608
23andMe allrs869025608
SNP Nexus

SNPshotrs869025608
SNPdbers869025608
MSV3drs869025608
GWAS Ctlgrs869025608
Max Magnitude0
ClinVar
Risk rs869025608(T;T)
Alt rs869025608(T;T)
Reference rs869025608(G;G)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome
Variation info
Gene MAP2K1
CLNDBN Cardiofaciocutaneous syndrome
Reversed 0
HGVS NC_000015.9:g.66727455G>T
CLNSRC
CLNACC RCV000208748.1,