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rs745683775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745683775(C;G)
Make rs745683775(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position46560448
GeneLOXHD1
is asnp
is mentioned by
dbSNPrs745683775
dbSNP (classic)rs745683775
ClinGenrs745683775
ebirs745683775
HLIrs745683775
Exacrs745683775
Gnomadrs745683775
Varsomers745683775
LitVarrs745683775
Maprs745683775
PheGenIrs745683775
Biobankrs745683775
1000 genomesrs745683775
hgdprs745683775
ensemblrs745683775
geneviewrs745683775
scholarrs745683775
googlers745683775
pharmgkbrs745683775
gwascentralrs745683775
openSNPrs745683775
23andMers745683775
SNPshotrs745683775
SNPdbers745683775
MSV3drs745683775
GWAS Ctlgrs745683775
Max Magnitude0
ClinVar
Risk rs745683775(G;G) rs745683775(T;T)
Alt rs745683775(G;G) rs745683775(T;T)
Reference Rs745683775(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene LOXHD1
CLNDBN not specified not provided
Reversed 0
HGVS NC_000018.9:g.44140411C>G
CLNSRC
CLNACC RCV000219519.1, RCV000485022.1,