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rs730880522

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880522(A;A)
Make rs730880522(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position4099333
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs730880522
ebirs730880522
HLIrs730880522
Exacrs730880522
Varsomers730880522
Maprs730880522
PheGenIrs730880522
hapmaprs730880522
1000 genomesrs730880522
hgdprs730880522
ensemblrs730880522
gopubmedrs730880522
geneviewrs730880522
scholarrs730880522
googlers730880522
pharmgkbrs730880522
gwascentralrs730880522
openSNPrs730880522
23andMers730880522
23andMe allrs730880522
SNP Nexus

SNPshotrs730880522
SNPdbers730880522
MSV3drs730880522
GWAS Ctlgrs730880522
Max Magnitude0
ClinVar
Risk rs730880522(A;A)
Alt rs730880522(A;A)
Reference rs730880522(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP2K2
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.4099331C>T
CLNSRC
CLNACC RCV000158047.2,