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

rs587777368

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777368(A;A)
Make rs587777368(A;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position17259462
GeneXYLT1
is asnp
is mentioned by
dbSNPrs587777368
ebirs587777368
HLIrs587777368
Exacrs587777368
Varsomers587777368
Maprs587777368
PheGenIrs587777368
hapmaprs587777368
1000 genomesrs587777368
hgdprs587777368
ensemblrs587777368
gopubmedrs587777368
geneviewrs587777368
scholarrs587777368
googlers587777368
pharmgkbrs587777368
gwascentralrs587777368
openSNPrs587777368
23andMers587777368
23andMe allrs587777368
SNP Nexus

SNPshotrs587777368
SNPdbers587777368
MSV3drs587777368
GWAS Ctlgrs587777368
Max Magnitude0
ClinVar
Risk rs587777368(A;A)
Alt rs587777368(A;A)
Reference rs587777368(G;G)
Significance Pathogenic
Disease Desbuquois dysplasia 2
Variation info
Gene XYLT1
CLNDBN Desbuquois dysplasia 2
Reversed 0
HGVS NC_000016.9:g.17353319G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000115035.2,