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rs387906541

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs387906541(-;-)
Make rs387906541(-;CT)
ReferenceGRCh38 38.1/141
Chromosome1
Position154601700
GeneADAR
is asnp
is mentioned by
dbSNPrs387906541
ebirs387906541
HLIrs387906541
Exacrs387906541
Varsomers387906541
Maprs387906541
PheGenIrs387906541
hapmaprs387906541
1000 genomesrs387906541
hgdprs387906541
ensemblrs387906541
gopubmedrs387906541
geneviewrs387906541
scholarrs387906541
googlers387906541
pharmgkbrs387906541
gwascentralrs387906541
openSNPrs387906541
23andMers387906541
23andMe allrs387906541
SNP Nexus

SNPshotrs387906541
SNPdbers387906541
MSV3drs387906541
GWAS Ctlgrs387906541
Max Magnitude0
ClinVar
Risk rs387906541(;)
Alt rs387906541(;)
Reference rs387906541(CT;CT)
Significance Pathogenic
Disease Symmetrical dyschromatosis of extremities
Variation info
Gene ADAR
CLNDBN Symmetrical dyschromatosis of extremities
Reversed 1
HGVS NC_000001.10:g.154574176_154574177delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000015945.26,