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rs1064796889

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome11
Position64804789
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs1064796889
dbSNP (classic)rs1064796889
ClinGenrs1064796889
ebirs1064796889
HLIrs1064796889
Exacrs1064796889
Gnomadrs1064796889
Varsomers1064796889
LitVarrs1064796889
Maprs1064796889
PheGenIrs1064796889
Biobankrs1064796889
1000 genomesrs1064796889
hgdprs1064796889
ensemblrs1064796889
geneviewrs1064796889
scholarrs1064796889
googlers1064796889
pharmgkbrs1064796889
gwascentralrs1064796889
openSNPrs1064796889
23andMers1064796889
23andMe allrs1064796889
SNPshotrs1064796889
SNPdbers1064796889
MSV3drs1064796889
GWAS Ctlgrs1064796889
Max Magnitude0
ClinVar
Risk rs1064796889(ACATAGT;ACATAGT)
Alt rs1064796889(ACATAGT;ACATAGT)
Reference Rs1064796889(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572261delGinsACTATGT
CLNSRC
CLNACC RCV000486244.1,