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

rs747523570

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747523570(A;A)
Make rs747523570(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position86718086
GeneLDB3
is asnp
is mentioned by
dbSNPrs747523570
dbSNP (classic)rs747523570
ClinGenrs747523570
ebirs747523570
HLIrs747523570
Exacrs747523570
Gnomadrs747523570
Varsomers747523570
LitVarrs747523570
Maprs747523570
PheGenIrs747523570
Biobankrs747523570
1000 genomesrs747523570
hgdprs747523570
ensemblrs747523570
geneviewrs747523570
scholarrs747523570
googlers747523570
pharmgkbrs747523570
gwascentralrs747523570
openSNPrs747523570
23andMers747523570
SNPshotrs747523570
SNPdbers747523570
MSV3drs747523570
GWAS Ctlgrs747523570
Max Magnitude0
ClinVar
Risk rs747523570(A;A) rs747523570(C;C)
Alt rs747523570(A;A) rs747523570(C;C)
Reference Rs747523570(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene LDB3
CLNDBN not specified not provided
Reversed 0
HGVS NC_000010.10:g.88477843G>A; NC_000010.10:g.88477843G>C
CLNSRC
CLNACC RCV000183541.2, RCV000171181.1,