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rs797044907

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044907(-;AGCT)
Make rs797044907(AGCT;AGCT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position72108662
GeneANAPC15, LRTOMT
is asnp
is mentioned by
dbSNPrs797044907
dbSNP (old)rs797044907
ClinGenrs797044907
ebirs797044907
HLIrs797044907
Exacrs797044907
Varsomers797044907
Maprs797044907
PheGenIrs797044907
Biobankrs797044907
1000 genomesrs797044907
hgdprs797044907
ensemblrs797044907
gopubmedrs797044907
geneviewrs797044907
scholarrs797044907
googlers797044907
pharmgkbrs797044907
gwascentralrs797044907
openSNPrs797044907
23andMers797044907
23andMe allrs797044907
SNP Nexus

SNPshotrs797044907
SNPdbers797044907
MSV3drs797044907
GWAS Ctlgrs797044907
Max Magnitude0
ClinVar
Risk rs797044907(AGCT;AGCT)
Alt rs797044907(AGCT;AGCT)
Reference Rs797044907(-;-)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ANAPC15 LRTOMT
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000011.9:g.71819708_71819709insAGCT
CLNSRC
CLNACC RCV000190734.1,