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rs1057518387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518387(-;AGCTC)
Make rs1057518387(AGCTC;AGCTC)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position157167180
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057518387
dbSNP (old)rs1057518387
ClinGenrs1057518387
ebirs1057518387
HLIrs1057518387
Exacrs1057518387
Gnomadrs1057518387
Varsomers1057518387
LitVarrs1057518387
Maprs1057518387
PheGenIrs1057518387
Biobankrs1057518387
1000 genomesrs1057518387
hgdprs1057518387
ensemblrs1057518387
gopubmedrs1057518387
geneviewrs1057518387
scholarrs1057518387
googlers1057518387
pharmgkbrs1057518387
gwascentralrs1057518387
openSNPrs1057518387
23andMers1057518387
23andMe allrs1057518387
SNPshotrs1057518387
SNPdbers1057518387
MSV3drs1057518387
GWAS Ctlgrs1057518387
Max Magnitude0
ClinVar
Risk rs1057518387(CAGCT;CAGCT)
Alt rs1057518387(CAGCT;CAGCT)
Reference Rs1057518387(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157488310_157488314dupAGCTC
CLNSRC
CLNACC RCV000412913.1,