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rs749272546

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749272546(-;-)
Make rs749272546(-;C)
ReferenceGRCh38.p7 38.3/149
Chromosome6
Position69701470
GeneLMBRD1
is asnp
is mentioned by
dbSNPrs749272546
dbSNP (classic)rs749272546
ClinGenrs749272546
ebirs749272546
HLIrs749272546
Exacrs749272546
Gnomadrs749272546
Varsomers749272546
LitVarrs749272546
Maprs749272546
PheGenIrs749272546
Biobankrs749272546
1000 genomesrs749272546
hgdprs749272546
ensemblrs749272546
geneviewrs749272546
scholarrs749272546
googlers749272546
pharmgkbrs749272546
gwascentralrs749272546
openSNPrs749272546
23andMers749272546
SNPshotrs749272546
SNPdbers749272546
MSV3drs749272546
GWAS Ctlgrs749272546
Max Magnitude0
ClinVar
Risk rs749272546(-;-)
Alt rs749272546(-;-)
Reference Rs749272546(C;C)
Significance Pathogenic
Disease Inborn genetic diseases not provided
Variation info
Gene LMBRD1
CLNDBN Inborn genetic diseases not provided
Reversed 0
HGVS NC_000006.11:g.70411362delC
CLNSRC
CLNACC RCV000210618.1, RCV000255705.1,