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rs1057518648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518648(A;A)
Make rs1057518648(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position156777946
GeneARID1B
is asnp
is mentioned by
dbSNPrs1057518648
dbSNP (old)rs1057518648
ClinGenrs1057518648
ebirs1057518648
HLIrs1057518648
Exacrs1057518648
Gnomadrs1057518648
Varsomers1057518648
Maprs1057518648
PheGenIrs1057518648
Biobankrs1057518648
1000 genomesrs1057518648
hgdprs1057518648
ensemblrs1057518648
gopubmedrs1057518648
geneviewrs1057518648
scholarrs1057518648
googlers1057518648
pharmgkbrs1057518648
gwascentralrs1057518648
openSNPrs1057518648
23andMers1057518648
23andMe allrs1057518648
SNPshotrs1057518648
SNPdbers1057518648
MSV3drs1057518648
GWAS Ctlgrs1057518648
Max Magnitude0
ClinVar
Risk rs1057518648(A;A)
Alt rs1057518648(A;A)
Reference Rs1057518648(G;G)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene ARID1B
CLNDBN Mental retardation, autosomal dominant 12
Reversed 0
HGVS NC_000006.11:g.157099080G>A
CLNSRC
CLNACC RCV000414923.1,