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rs1060505022

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060505022(-;-)
Make rs1060505022(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position119091154
GeneCOLEC10
is asnp
is mentioned by
dbSNPrs1060505022
dbSNP (classic)rs1060505022
ClinGenrs1060505022
ebirs1060505022
HLIrs1060505022
Exacrs1060505022
Gnomadrs1060505022
Varsomers1060505022
LitVarrs1060505022
Maprs1060505022
PheGenIrs1060505022
Biobankrs1060505022
1000 genomesrs1060505022
hgdprs1060505022
ensemblrs1060505022
geneviewrs1060505022
scholarrs1060505022
googlers1060505022
pharmgkbrs1060505022
gwascentralrs1060505022
openSNPrs1060505022
23andMers1060505022
23andMe allrs1060505022
SNPshotrs1060505022
SNPdbers1060505022
MSV3drs1060505022
GWAS Ctlgrs1060505022
Max Magnitude0
ClinVar
Risk rs1060505022(-;-)
Alt rs1060505022(-;-)
Reference Rs1060505022(A;A)
Significance Pathogenic
Disease Malpuech facial clefting syndrome
Variation info
Gene COLEC10
CLNDBN Malpuech facial clefting syndrome
Reversed 0
HGVS NC_000008.10:g.120103393delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000477723.1,