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rs1057518059

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518059(G;T)
Make rs1057518059(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position157174030
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057518059
dbSNP (old)rs1057518059
ClinGenrs1057518059
ebirs1057518059
HLIrs1057518059
Exacrs1057518059
Gnomadrs1057518059
Varsomers1057518059
Maprs1057518059
PheGenIrs1057518059
Biobankrs1057518059
1000 genomesrs1057518059
hgdprs1057518059
ensemblrs1057518059
gopubmedrs1057518059
geneviewrs1057518059
scholarrs1057518059
googlers1057518059
pharmgkbrs1057518059
gwascentralrs1057518059
openSNPrs1057518059
23andMers1057518059
23andMe allrs1057518059
SNPshotrs1057518059
SNPdbers1057518059
MSV3drs1057518059
GWAS Ctlgrs1057518059
Max Magnitude0
ClinVar
Risk rs1057518059(T;T)
Alt rs1057518059(T;T)
Reference Rs1057518059(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157495164G>T
CLNSRC
CLNACC RCV000413584.1,