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rs886037756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs886037756(-;GTGAACC)
Make rs886037756(GTGAACC;GTGAACC)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position100749759
GenePAX2
is asnp
is mentioned by
dbSNPrs886037756
dbSNP (classic)rs886037756
ClinGenrs886037756
ebirs886037756
HLIrs886037756
Exacrs886037756
Gnomadrs886037756
Varsomers886037756
LitVarrs886037756
Maprs886037756
PheGenIrs886037756
Biobankrs886037756
1000 genomesrs886037756
hgdprs886037756
ensemblrs886037756
geneviewrs886037756
scholarrs886037756
googlers886037756
pharmgkbrs886037756
gwascentralrs886037756
openSNPrs886037756
23andMers886037756
23andMe allrs886037756
SNPshotrs886037756
SNPdbers886037756
MSV3drs886037756
GWAS Ctlgrs886037756
Max Magnitude0
ClinVar
Risk rs886037756(GTGAACC;GTGAACC)
Alt rs886037756(GTGAACC;GTGAACC)
Reference Rs886037756(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX2
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.102509516_102509517insGTGAACC
CLNSRC
CLNACC RCV000240647.1,