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rs886037757

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs886037757(-;AC)
Make rs886037757(AC;AC)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position100750705
GenePAX2
is asnp
is mentioned by
dbSNPrs886037757
dbSNP (classic)rs886037757
ClinGenrs886037757
ebirs886037757
HLIrs886037757
Exacrs886037757
Gnomadrs886037757
Varsomers886037757
LitVarrs886037757
Maprs886037757
PheGenIrs886037757
Biobankrs886037757
1000 genomesrs886037757
hgdprs886037757
ensemblrs886037757
geneviewrs886037757
scholarrs886037757
googlers886037757
pharmgkbrs886037757
gwascentralrs886037757
openSNPrs886037757
23andMers886037757
23andMe allrs886037757
SNPshotrs886037757
SNPdbers886037757
MSV3drs886037757
GWAS Ctlgrs886037757
Max Magnitude0
ClinVar
Risk rs886037757(AC;AC)
Alt rs886037757(AC;AC)
Reference Rs886037757(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102510461_102510462dupAC
CLNSRC
CLNACC RCV000240626.1,