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rs1127313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1127313(C;T)
Make rs1127313(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position154583949
GeneADAR
is asnp
is mentioned by
dbSNPrs1127313
dbSNP (classic)rs1127313
ClinGenrs1127313
ebirs1127313
HLIrs1127313
Exacrs1127313
Gnomadrs1127313
Varsomers1127313
LitVarrs1127313
Maprs1127313
PheGenIrs1127313
Biobankrs1127313
1000 genomesrs1127313
hgdprs1127313
ensemblrs1127313
geneviewrs1127313
scholarrs1127313
googlers1127313
pharmgkbrs1127313
gwascentralrs1127313
openSNPrs1127313
23andMers1127313
23andMe allrs1127313
SNPshotrs1127313
SNPdbers1127313
MSV3drs1127313
GWAS Ctlgrs1127313
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 27911851OA-icon.png] Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration.


ClinVar
Risk rs1127313(T;T)
Alt rs1127313(T;T)
Reference Rs1127313(C;C)
Significance Non-pathogenic
Disease Symmetrical dyschromatosis of extremities
Variation info
Gene ADAR
CLNDBN Symmetrical dyschromatosis of extremities
Reversed 1
HGVS NC_000001.10:g.154556425G>A
CLNSRC
CLNACC RCV000301586.1,