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rs387907163

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907163(A;T)
Make rs387907163(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position1349792
GeneUVSSA
is asnp
is mentioned by
dbSNPrs387907163
ebirs387907163
HLIrs387907163
Exacrs387907163
Varsomers387907163
Maprs387907163
PheGenIrs387907163
hapmaprs387907163
1000 genomesrs387907163
hgdprs387907163
ensemblrs387907163
gopubmedrs387907163
geneviewrs387907163
scholarrs387907163
googlers387907163
pharmgkbrs387907163
gwascentralrs387907163
openSNPrs387907163
23andMers387907163
23andMe allrs387907163
SNP Nexus

SNPshotrs387907163
SNPdbers387907163
MSV3drs387907163
GWAS Ctlgrs387907163
Max Magnitude0
ClinVar
Risk rs387907163(T;T)
Alt rs387907163(T;T)
Reference rs387907163(A;A)
Significance Pathogenic
Disease UV-sensitive syndrome 3
Variation info
Gene UVSSA
CLNDBN UV-sensitive syndrome 3
Reversed 0
HGVS NC_000004.11:g.1343580A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024277.2,