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rs749681373

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs749681373(-;G)
Make rs749681373(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position31562160
GeneLOC105370437, NUBPL
is asnp
is mentioned by
dbSNPrs749681373
dbSNP (old)rs749681373
ClinGenrs749681373
ebirs749681373
HLIrs749681373
Exacrs749681373
Gnomadrs749681373
Varsomers749681373
Maprs749681373
PheGenIrs749681373
Biobankrs749681373
1000 genomesrs749681373
hgdprs749681373
ensemblrs749681373
gopubmedrs749681373
geneviewrs749681373
scholarrs749681373
googlers749681373
pharmgkbrs749681373
gwascentralrs749681373
openSNPrs749681373
23andMers749681373
23andMe allrs749681373
SNP Nexus

SNPshotrs749681373
SNPdbers749681373
MSV3drs749681373
GWAS Ctlgrs749681373
Max Magnitude0
ClinVar
Risk rs749681373(G;G)
Alt rs749681373(G;G)
Reference Rs749681373(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene NUBPL
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.32031366_32031367insG
CLNSRC
CLNACC RCV000200167.1,