Have questions? Visit https://www.reddit.com/r/SNPedia

rs886039372

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039372(-;-)
Make rs886039372(-;C)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position86952468
GeneFZD4, PRSS23
is asnp
is mentioned by
dbSNPrs886039372
dbSNP (classic)rs886039372
ClinGenrs886039372
ebirs886039372
HLIrs886039372
Exacrs886039372
Gnomadrs886039372
Varsomers886039372
LitVarrs886039372
Maprs886039372
PheGenIrs886039372
Biobankrs886039372
1000 genomesrs886039372
hgdprs886039372
ensemblrs886039372
geneviewrs886039372
scholarrs886039372
googlers886039372
pharmgkbrs886039372
gwascentralrs886039372
openSNPrs886039372
23andMers886039372
SNPshotrs886039372
SNPdbers886039372
MSV3drs886039372
GWAS Ctlgrs886039372
Max Magnitude0
ClinVar
Risk rs886039372(-;-)
Alt rs886039372(-;-)
Reference Rs886039372(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PRSS23 FZD4
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.86663510delG
CLNSRC
CLNACC RCV000254871.1,