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rs775225727

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs775225727(A;A)
Make rs775225727(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position69599802
GeneAUTS2
is asnp
is mentioned by
dbSNPrs775225727
dbSNP (classic)rs775225727
ClinGenrs775225727
ebirs775225727
HLIrs775225727
Exacrs775225727
Gnomadrs775225727
Varsomers775225727
LitVarrs775225727
Maprs775225727
PheGenIrs775225727
Biobankrs775225727
1000 genomesrs775225727
hgdprs775225727
ensemblrs775225727
geneviewrs775225727
scholarrs775225727
googlers775225727
pharmgkbrs775225727
gwascentralrs775225727
openSNPrs775225727
23andMers775225727
23andMe allrs775225727
SNPshotrs775225727
SNPdbers775225727
MSV3drs775225727
GWAS Ctlgrs775225727
Max Magnitude0
ClinVar
Risk rs775225727(A;A) rs775225727(G;G)
Alt rs775225727(A;A) rs775225727(G;G)
Reference Rs775225727(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AUTS2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.69064788C>A
CLNSRC
CLNACC RCV000440958.1,