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rs886037754

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs886037754(-;-)
Make rs886037754(-;GC)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position100749821
GenePAX2
is asnp
is mentioned by
dbSNPrs886037754
dbSNP (classic)rs886037754
ClinGenrs886037754
ebirs886037754
HLIrs886037754
Exacrs886037754
Gnomadrs886037754
Varsomers886037754
LitVarrs886037754
Maprs886037754
PheGenIrs886037754
Biobankrs886037754
1000 genomesrs886037754
hgdprs886037754
ensemblrs886037754
geneviewrs886037754
scholarrs886037754
googlers886037754
pharmgkbrs886037754
gwascentralrs886037754
openSNPrs886037754
23andMers886037754
23andMe allrs886037754
SNPshotrs886037754
SNPdbers886037754
MSV3drs886037754
GWAS Ctlgrs886037754
Max Magnitude0
ClinVar
Risk rs886037754(-;-)
Alt rs886037754(-;-)
Reference Rs886037754(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102509578_102509579delGC
CLNSRC
CLNACC RCV000240627.1,