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rs587777370

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777370(G;G)
Make rs587777370(G;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position17158911
GeneXYLT1
is asnp
is mentioned by
dbSNPrs587777370
ebirs587777370
HLIrs587777370
Exacrs587777370
Varsomers587777370
Maprs587777370
PheGenIrs587777370
hapmaprs587777370
1000 genomesrs587777370
hgdprs587777370
ensemblrs587777370
gopubmedrs587777370
geneviewrs587777370
scholarrs587777370
googlers587777370
pharmgkbrs587777370
gwascentralrs587777370
openSNPrs587777370
23andMers587777370
23andMe allrs587777370
SNP Nexus

SNPshotrs587777370
SNPdbers587777370
MSV3drs587777370
GWAS Ctlgrs587777370
Max Magnitude0
ClinVar
Risk rs587777370(G,T;G,T)
Alt rs587777370(G,T;G,T)
Reference rs587777370(A;A)
Significance Pathogenic
Disease Desbuquois dysplasia 2
Variation info
Gene XYLT1
CLNDBN Desbuquois dysplasia 2
Reversed 1
HGVS NC_000016.9:g.17252768T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000115038.2,