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rs1057524755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524755(A;A)
Make rs1057524755(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position46524602
GeneLOXHD1
is asnp
is mentioned by
dbSNPrs1057524755
dbSNP (old)rs1057524755
ClinGenrs1057524755
ebirs1057524755
HLIrs1057524755
Exacrs1057524755
Gnomadrs1057524755
Varsomers1057524755
LitVarrs1057524755
Maprs1057524755
PheGenIrs1057524755
Biobankrs1057524755
1000 genomesrs1057524755
hgdprs1057524755
ensemblrs1057524755
gopubmedrs1057524755
geneviewrs1057524755
scholarrs1057524755
googlers1057524755
pharmgkbrs1057524755
gwascentralrs1057524755
openSNPrs1057524755
23andMers1057524755
23andMe allrs1057524755
SNPshotrs1057524755
SNPdbers1057524755
MSV3drs1057524755
GWAS Ctlgrs1057524755
Max Magnitude0
ClinVar
Risk rs1057524755(A;A)
Alt rs1057524755(A;A)
Reference Rs1057524755(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOXHD1
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.44104565C>T
CLNSRC
CLNACC RCV000419915.1,