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rs201128942

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201128942(A;A)
Make rs201128942(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position85547112
GeneSNX14
is asnp
is mentioned by
dbSNPrs201128942
dbSNP (old)rs201128942
ClinGenrs201128942
ebirs201128942
HLIrs201128942
Exacrs201128942
Gnomadrs201128942
Varsomers201128942
LitVarrs201128942
Maprs201128942
PheGenIrs201128942
Biobankrs201128942
1000 genomesrs201128942
hgdprs201128942
ensemblrs201128942
gopubmedrs201128942
geneviewrs201128942
scholarrs201128942
googlers201128942
pharmgkbrs201128942
gwascentralrs201128942
openSNPrs201128942
23andMers201128942
23andMe allrs201128942
SNPshotrs201128942
SNPdbers201128942
MSV3drs201128942
GWAS Ctlgrs201128942
Max Magnitude0
ClinVar
Risk rs201128942(A;A)
Alt rs201128942(A;A)
Reference Rs201128942(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SNX14
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.86256830C>A
CLNSRC
CLNACC RCV000413946.1,