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rs730880504

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880504(A;A)
Make rs730880504(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position66436866
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs730880504
ebirs730880504
HLIrs730880504
Exacrs730880504
Varsomers730880504
Maprs730880504
PheGenIrs730880504
hapmaprs730880504
1000 genomesrs730880504
hgdprs730880504
ensemblrs730880504
gopubmedrs730880504
geneviewrs730880504
scholarrs730880504
googlers730880504
pharmgkbrs730880504
gwascentralrs730880504
openSNPrs730880504
23andMers730880504
23andMe allrs730880504
SNP Nexus

SNPshotrs730880504
SNPdbers730880504
MSV3drs730880504
GWAS Ctlgrs730880504
Max Magnitude0
ClinVar
Risk rs730880504(A;A)
Alt rs730880504(A;A)
Reference rs730880504(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MAP2K1
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.66729204G>A
CLNSRC
CLNACC RCV000158009.2,