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rs876657651

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657651(A;G)
Make rs876657651(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position66436818
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs876657651
ebirs876657651
HLIrs876657651
Exacrs876657651
Varsomers876657651
Maprs876657651
PheGenIrs876657651
hapmaprs876657651
1000 genomesrs876657651
hgdprs876657651
ensemblrs876657651
gopubmedrs876657651
geneviewrs876657651
scholarrs876657651
googlers876657651
pharmgkbrs876657651
gwascentralrs876657651
openSNPrs876657651
23andMers876657651
23andMe allrs876657651
SNP Nexus

SNPshotrs876657651
SNPdbers876657651
MSV3drs876657651
GWAS Ctlgrs876657651
Max Magnitude0
ClinVar
Risk rs876657651(G;G)
Alt rs876657651(G;G)
Reference rs876657651(A;A)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene MAP2K1
CLNDBN Rasopathy
Reversed 0
HGVS NC_000015.9:g.66729156A>G
CLNSRC
CLNACC RCV000220187.1,