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rs483352913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs483352913(A;A)
Make rs483352913(A;G)
ReferenceGRCh38 38.1/142
Chromosome15
Position58621471
GeneADAM10
is asnp
is mentioned by
dbSNPrs483352913
ebirs483352913
HLIrs483352913
Exacrs483352913
Varsomers483352913
Maprs483352913
PheGenIrs483352913
hapmaprs483352913
1000 genomesrs483352913
hgdprs483352913
ensemblrs483352913
gopubmedrs483352913
geneviewrs483352913
scholarrs483352913
googlers483352913
pharmgkbrs483352913
gwascentralrs483352913
openSNPrs483352913
23andMers483352913
23andMe allrs483352913
SNP Nexus

SNPshotrs483352913
SNPdbers483352913
MSV3drs483352913
GWAS Ctlgrs483352913
Max Magnitude0
ClinVar
Risk rs483352913(A;A)
Alt rs483352913(A;A)
Reference rs483352913(G;G)
Significance Pathogenic
Disease Reticulate acropigmentation of Kitamura
Variation info
Gene ADAM10
CLNDBN Reticulate acropigmentation of Kitamura
Reversed 1
HGVS NC_000015.9:g.58913670C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074428.3,