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rs886037755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886037755(A;A)
Make rs886037755(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position100749889
GenePAX2
is asnp
is mentioned by
dbSNPrs886037755
dbSNP (classic)rs886037755
ClinGenrs886037755
ebirs886037755
HLIrs886037755
Exacrs886037755
Gnomadrs886037755
Varsomers886037755
LitVarrs886037755
Maprs886037755
PheGenIrs886037755
Biobankrs886037755
1000 genomesrs886037755
hgdprs886037755
ensemblrs886037755
geneviewrs886037755
scholarrs886037755
googlers886037755
pharmgkbrs886037755
gwascentralrs886037755
openSNPrs886037755
23andMers886037755
23andMe allrs886037755
SNPshotrs886037755
SNPdbers886037755
MSV3drs886037755
GWAS Ctlgrs886037755
Max Magnitude0
ClinVar
Risk rs886037755(A;A)
Alt rs886037755(A;A)
Reference Rs886037755(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102509646G>A
CLNSRC
CLNACC RCV000240634.1,