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rs730880507

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880507(G;G)
Make rs730880507(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position66485026
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs730880507
ebirs730880507
HLIrs730880507
Exacrs730880507
Varsomers730880507
Maprs730880507
PheGenIrs730880507
hapmaprs730880507
1000 genomesrs730880507
hgdprs730880507
ensemblrs730880507
gopubmedrs730880507
geneviewrs730880507
scholarrs730880507
googlers730880507
pharmgkbrs730880507
gwascentralrs730880507
openSNPrs730880507
23andMers730880507
23andMe allrs730880507
SNP Nexus

SNPshotrs730880507
SNPdbers730880507
MSV3drs730880507
GWAS Ctlgrs730880507
Max Magnitude0
ClinVar
Risk rs730880507(G;G)
Alt rs730880507(G;G)
Reference rs730880507(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP2K1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.66777364T>G
CLNSRC
CLNACC RCV000158012.1,