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rs2075702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2075702(C;C)
Make rs2075702(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31969734
GeneDXO, SKIV2L, STK19
is asnp
is mentioned by
dbSNPrs2075702
dbSNP (classic)rs2075702
ClinGenrs2075702
ebirs2075702
HLIrs2075702
Exacrs2075702
Gnomadrs2075702
Varsomers2075702
LitVarrs2075702
Maprs2075702
PheGenIrs2075702
Biobankrs2075702
1000 genomesrs2075702
hgdprs2075702
ensemblrs2075702
geneviewrs2075702
scholarrs2075702
googlers2075702
pharmgkbrs2075702
gwascentralrs2075702
openSNPrs2075702
23andMers2075702
SNPshotrs2075702
SNPdbers2075702
MSV3drs2075702
GWAS Ctlgrs2075702
GMAF0.01056
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 19556007] Role of RDBP and SKIV2L variants in the major histocompatibility complex class III region in polypoidal choroidal vasculopathy etiology


ClinVar
Risk rs2075702(C;C)
Alt rs2075702(C;C)
Reference Rs2075702(T;T)
Significance Probable-non-pathogenic
Disease Trichohepatoenteric syndrome
Variation info
Gene DXO STK19 SKIV2L
CLNDBN Trichohepatoenteric syndrome
Reversed 0
HGVS NC_000006.11:g.31937511T>C
CLNSRC
CLNACC RCV000294596.1,