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rs1057521854

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521854(C;C)
Make rs1057521854(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position157207547
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057521854
dbSNP (old)rs1057521854
ClinGenrs1057521854
ebirs1057521854
HLIrs1057521854
Exacrs1057521854
Gnomadrs1057521854
Varsomers1057521854
Maprs1057521854
PheGenIrs1057521854
Biobankrs1057521854
1000 genomesrs1057521854
hgdprs1057521854
ensemblrs1057521854
gopubmedrs1057521854
geneviewrs1057521854
scholarrs1057521854
googlers1057521854
pharmgkbrs1057521854
gwascentralrs1057521854
openSNPrs1057521854
23andMers1057521854
23andMe allrs1057521854
SNPshotrs1057521854
SNPdbers1057521854
MSV3drs1057521854
GWAS Ctlgrs1057521854
Max Magnitude0
ClinVar
Risk rs1057521854(C;C)
Alt rs1057521854(C;C)
Reference Rs1057521854(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157528681T>C
CLNSRC
CLNACC RCV000442247.1,