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rs587777369

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777369(-;-)
Make rs587777369(-;C)
Make rs587777369(C;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position17470521
GeneXYLT1
is asnp
is mentioned by
dbSNPrs587777369
ebirs587777369
HLIrs587777369
Exacrs587777369
Varsomers587777369
Maprs587777369
PheGenIrs587777369
hapmaprs587777369
1000 genomesrs587777369
hgdprs587777369
ensemblrs587777369
gopubmedrs587777369
geneviewrs587777369
scholarrs587777369
googlers587777369
pharmgkbrs587777369
gwascentralrs587777369
openSNPrs587777369
23andMers587777369
23andMe allrs587777369
SNP Nexus

SNPshotrs587777369
SNPdbers587777369
MSV3drs587777369
GWAS Ctlgrs587777369
Max Magnitude0
ClinVar
Risk rs587777369(C;C)
Alt rs587777369(C;C)
Reference rs587777369(;)
Significance Pathogenic
Disease Desbuquois dysplasia 2
Variation info
Gene XYLT1
CLNDBN Desbuquois dysplasia 2
Reversed 0
HGVS NC_000016.9:g.17564378dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000115036.2,