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rs797044859

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs797044859(-;-)
Make rs797044859(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position157200765
GeneARID1B
is asnp
is mentioned by
dbSNPrs797044859
dbSNP (old)rs797044859
ClinGenrs797044859
ebirs797044859
HLIrs797044859
Exacrs797044859
Gnomadrs797044859
Varsomers797044859
Maprs797044859
PheGenIrs797044859
Biobankrs797044859
1000 genomesrs797044859
hgdprs797044859
ensemblrs797044859
gopubmedrs797044859
geneviewrs797044859
scholarrs797044859
googlers797044859
pharmgkbrs797044859
gwascentralrs797044859
openSNPrs797044859
23andMers797044859
23andMe allrs797044859
SNP Nexus

SNPshotrs797044859
SNPdbers797044859
MSV3drs797044859
GWAS Ctlgrs797044859
Max Magnitude0
ClinVar
Risk rs797044859(-;-)
Alt rs797044859(-;-)
Reference Rs797044859(AT;AT)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ARID1B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000006.11:g.157521899_157521900delAT
CLNSRC
CLNACC RCV000190662.1,