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rs539555837

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs539555837(C;C)
Make rs539555837(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position4099302
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs539555837
ebirs539555837
HLIrs539555837
Exacrs539555837
Varsomers539555837
Maprs539555837
PheGenIrs539555837
hapmaprs539555837
1000 genomesrs539555837
hgdprs539555837
ensemblrs539555837
gopubmedrs539555837
geneviewrs539555837
scholarrs539555837
googlers539555837
pharmgkbrs539555837
gwascentralrs539555837
openSNPrs539555837
23andMers539555837
23andMe allrs539555837
SNP Nexus

SNPshotrs539555837
SNPdbers539555837
MSV3drs539555837
GWAS Ctlgrs539555837
Max Magnitude0
ClinVar
Risk rs539555837(C;C)
Alt rs539555837(C;C)
Reference rs539555837(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MAP2K2
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.4099300T>C
CLNSRC
CLNACC RCV000158027.2,