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rs1057518213

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518213(C;T)
Make rs1057518213(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position156779289
GeneARID1B, MIR4466
is asnp
is mentioned by
dbSNPrs1057518213
dbSNP (old)rs1057518213
ClinGenrs1057518213
ebirs1057518213
HLIrs1057518213
Exacrs1057518213
Gnomadrs1057518213
Varsomers1057518213
Maprs1057518213
PheGenIrs1057518213
Biobankrs1057518213
1000 genomesrs1057518213
hgdprs1057518213
ensemblrs1057518213
gopubmedrs1057518213
geneviewrs1057518213
scholarrs1057518213
googlers1057518213
pharmgkbrs1057518213
gwascentralrs1057518213
openSNPrs1057518213
23andMers1057518213
23andMe allrs1057518213
SNPshotrs1057518213
SNPdbers1057518213
MSV3drs1057518213
GWAS Ctlgrs1057518213
Max Magnitude0
ClinVar
Risk rs1057518213(T;T)
Alt rs1057518213(T;T)
Reference Rs1057518213(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR4466 ARID1B
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.157100423C>T
CLNSRC
CLNACC RCV000413510.1,