Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517704(C;T)
Make rs1057517704(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position157148848
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057517704
dbSNP (old)rs1057517704
ClinGenrs1057517704
ebirs1057517704
HLIrs1057517704
Exacrs1057517704
Gnomadrs1057517704
Varsomers1057517704
Maprs1057517704
PheGenIrs1057517704
Biobankrs1057517704
1000 genomesrs1057517704
hgdprs1057517704
ensemblrs1057517704
gopubmedrs1057517704
geneviewrs1057517704
scholarrs1057517704
googlers1057517704
pharmgkbrs1057517704
gwascentralrs1057517704
openSNPrs1057517704
23andMers1057517704
23andMe allrs1057517704
SNPshotrs1057517704
SNPdbers1057517704
MSV3drs1057517704
GWAS Ctlgrs1057517704
Max Magnitude0
ClinVar
Risk rs1057517704(T;T)
Alt rs1057517704(T;T)
Reference Rs1057517704(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157469982C>T
CLNSRC
CLNACC RCV000413838.1,