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rs1085307563

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome16
Position17138385
GeneLOC102723692, XYLT1
is asnp
is mentioned by
dbSNPrs1085307563
dbSNP (old)rs1085307563
ClinGenrs1085307563
ebirs1085307563
HLIrs1085307563
Exacrs1085307563
Gnomadrs1085307563
Varsomers1085307563
LitVarrs1085307563
Maprs1085307563
PheGenIrs1085307563
Biobankrs1085307563
1000 genomesrs1085307563
hgdprs1085307563
ensemblrs1085307563
gopubmedrs1085307563
geneviewrs1085307563
scholarrs1085307563
googlers1085307563
pharmgkbrs1085307563
gwascentralrs1085307563
openSNPrs1085307563
23andMers1085307563
23andMe allrs1085307563
SNPshotrs1085307563
SNPdbers1085307563
MSV3drs1085307563
GWAS Ctlgrs1085307563
Max Magnitude0
ClinVar
Risk rs1085307563(ATGA;ATGA)
Alt rs1085307563(ATGA;ATGA)
Reference Rs1085307563(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102723692 XYLT1
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.17232243_17232246dup
CLNSRC
CLNACC RCV000489929.1,