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rs35441529

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs35441529(-;C)
Make rs35441529(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position157206688
GeneARID1B
is asnp
is mentioned by
dbSNPrs35441529
dbSNP (classic)rs35441529
ClinGenrs35441529
ebirs35441529
HLIrs35441529
Exacrs35441529
Gnomadrs35441529
Varsomers35441529
LitVarrs35441529
Maprs35441529
PheGenIrs35441529
Biobankrs35441529
1000 genomesrs35441529
hgdprs35441529
ensemblrs35441529
geneviewrs35441529
scholarrs35441529
googlers35441529
pharmgkbrs35441529
gwascentralrs35441529
openSNPrs35441529
23andMers35441529
SNPshotrs35441529
SNPdbers35441529
MSV3drs35441529
GWAS Ctlgrs35441529
Max Magnitude0
ClinVar
Risk rs35441529(C;C)
Alt rs35441529(C;C)
Reference Rs35441529(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157527822dupC
CLNSRC
CLNACC RCV000359978.1,