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rs1057519809

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519809(C;T)
Make rs1057519809(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position4117586
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs1057519809
dbSNP (old)rs1057519809
ClinGenrs1057519809
ebirs1057519809
HLIrs1057519809
Exacrs1057519809
Gnomadrs1057519809
Varsomers1057519809
Maprs1057519809
PheGenIrs1057519809
Biobankrs1057519809
1000 genomesrs1057519809
hgdprs1057519809
ensemblrs1057519809
gopubmedrs1057519809
geneviewrs1057519809
scholarrs1057519809
googlers1057519809
pharmgkbrs1057519809
gwascentralrs1057519809
openSNPrs1057519809
23andMers1057519809
23andMe allrs1057519809
SNPshotrs1057519809
SNPdbers1057519809
MSV3drs1057519809
GWAS Ctlgrs1057519809
Max Magnitude0
ClinVar
Risk rs1057519809(T;T)
Alt rs1057519809(T;T)
Reference Rs1057519809(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene MAP2K2
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000019.9:g.4117584G>A
CLNSRC
CLNACC RCV000432005.1,