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rs1064794799

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome6
Position157207265
GeneARID1B
is asnp
is mentioned by
dbSNPrs1064794799
dbSNP (classic)rs1064794799
ClinGenrs1064794799
ebirs1064794799
HLIrs1064794799
Exacrs1064794799
Gnomadrs1064794799
Varsomers1064794799
LitVarrs1064794799
Maprs1064794799
PheGenIrs1064794799
Biobankrs1064794799
1000 genomesrs1064794799
hgdprs1064794799
ensemblrs1064794799
geneviewrs1064794799
scholarrs1064794799
googlers1064794799
pharmgkbrs1064794799
gwascentralrs1064794799
openSNPrs1064794799
23andMers1064794799
SNPshotrs1064794799
SNPdbers1064794799
MSV3drs1064794799
GWAS Ctlgrs1064794799
Max Magnitude0
ClinVar
Risk rs1064794799(A;A)
Alt rs1064794799(A;A)
Reference Rs1064794799(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157528399G>A
CLNSRC
CLNACC RCV000486528.1,