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rs1057517708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517708(C;T)
Make rs1057517708(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position70766128
GeneAUTS2
is asnp
is mentioned by
dbSNPrs1057517708
dbSNP (old)rs1057517708
ClinGenrs1057517708
ebirs1057517708
HLIrs1057517708
Exacrs1057517708
Gnomadrs1057517708
Varsomers1057517708
LitVarrs1057517708
Maprs1057517708
PheGenIrs1057517708
Biobankrs1057517708
1000 genomesrs1057517708
hgdprs1057517708
ensemblrs1057517708
gopubmedrs1057517708
geneviewrs1057517708
scholarrs1057517708
googlers1057517708
pharmgkbrs1057517708
gwascentralrs1057517708
openSNPrs1057517708
23andMers1057517708
23andMe allrs1057517708
SNPshotrs1057517708
SNPdbers1057517708
MSV3drs1057517708
GWAS Ctlgrs1057517708
Max Magnitude0
ClinVar
Risk rs1057517708(T;T)
Alt rs1057517708(T;T)
Reference Rs1057517708(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene AUTS2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.70231114C>T
CLNSRC
CLNACC RCV000413202.1,