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rs797044807

From SNPedia

Orientationplus
Make rs797044807(-;-)
Make rs797044807(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position50354014
GeneXYLT2
is asnp
is mentioned by
dbSNPrs797044807
ebirs797044807
HLIrs797044807
Exacrs797044807
Varsomers797044807
Maprs797044807
PheGenIrs797044807
hapmaprs797044807
1000 genomesrs797044807
hgdprs797044807
ensemblrs797044807
gopubmedrs797044807
geneviewrs797044807
scholarrs797044807
googlers797044807
pharmgkbrs797044807
gwascentralrs797044807
openSNPrs797044807
23andMers797044807
23andMe allrs797044807
SNP Nexus

SNPshotrs797044807
SNPdbers797044807
MSV3drs797044807
GWAS Ctlgrs797044807
Max Magnitude
ClinVar
Risk rs797044807(;)
Alt rs797044807(;)
Reference rs797044807(G;G)
Significance Pathogenic
Disease Spondyloocular syndrome
Variation info
Gene XYLT2
CLNDBN Spondyloocular syndrome, autosomal recessive
Reversed 0
HGVS NC_000017.10:g.48431375delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000190244.2,