Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516790

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516790(A;C)
Make rs397516790(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position66435115
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs397516790
ebirs397516790
HLIrs397516790
Exacrs397516790
Varsomers397516790
Maprs397516790
PheGenIrs397516790
hapmaprs397516790
1000 genomesrs397516790
hgdprs397516790
ensemblrs397516790
gopubmedrs397516790
geneviewrs397516790
scholarrs397516790
googlers397516790
pharmgkbrs397516790
gwascentralrs397516790
openSNPrs397516790
23andMers397516790
23andMe allrs397516790
SNP Nexus

SNPshotrs397516790
SNPdbers397516790
MSV3drs397516790
GWAS Ctlgrs397516790
Max Magnitude0
ClinVar
Risk rs397516790(C;C)
Alt rs397516790(C;C)
Reference rs397516790(A;A)
Significance Probable-Pathogenic
Disease Cardiofaciocutaneous syndrome Rasopathy
Variation info
Gene MAP2K1
CLNDBN Cardiofaciocutaneous syndrome Rasopathy
Reversed 0
HGVS NC_000015.9:g.66727453A>C
CLNSRC ClinVar
CLNACC RCV000037591.3, RCV000158014.1,