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rs730880518

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880518(G;T)
Make rs730880518(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position4117532
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs730880518
ebirs730880518
HLIrs730880518
Exacrs730880518
Varsomers730880518
Maprs730880518
PheGenIrs730880518
hapmaprs730880518
1000 genomesrs730880518
hgdprs730880518
ensemblrs730880518
gopubmedrs730880518
geneviewrs730880518
scholarrs730880518
googlers730880518
pharmgkbrs730880518
gwascentralrs730880518
openSNPrs730880518
23andMers730880518
23andMe allrs730880518
SNP Nexus

SNPshotrs730880518
SNPdbers730880518
MSV3drs730880518
GWAS Ctlgrs730880518
Max Magnitude0
ClinVar
Risk rs730880518(T;T)
Alt rs730880518(T;T)
Reference rs730880518(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP2K2
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.4117530C>A
CLNSRC
CLNACC RCV000158040.1,