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rs1057518198

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518198(-;-)
Make rs1057518198(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position70764835
GeneAUTS2
is asnp
is mentioned by
dbSNPrs1057518198
dbSNP (old)rs1057518198
ClinGenrs1057518198
ebirs1057518198
HLIrs1057518198
Exacrs1057518198
Gnomadrs1057518198
Varsomers1057518198
Maprs1057518198
PheGenIrs1057518198
Biobankrs1057518198
1000 genomesrs1057518198
hgdprs1057518198
ensemblrs1057518198
gopubmedrs1057518198
geneviewrs1057518198
scholarrs1057518198
googlers1057518198
pharmgkbrs1057518198
gwascentralrs1057518198
openSNPrs1057518198
23andMers1057518198
23andMe allrs1057518198
SNPshotrs1057518198
SNPdbers1057518198
MSV3drs1057518198
GWAS Ctlgrs1057518198
Max Magnitude0
ClinVar
Risk rs1057518198(-;-)
Alt rs1057518198(-;-)
Reference Rs1057518198(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene AUTS2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.70229821delT
CLNSRC
CLNACC RCV000413601.1,