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rs483352914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs483352914(A;A)
Make rs483352914(A;T)
ReferenceGRCh38 38.1/142
Chromosome15
Position58679179
GeneADAM10
is asnp
is mentioned by
dbSNPrs483352914
ebirs483352914
HLIrs483352914
Exacrs483352914
Varsomers483352914
Maprs483352914
PheGenIrs483352914
hapmaprs483352914
1000 genomesrs483352914
hgdprs483352914
ensemblrs483352914
gopubmedrs483352914
geneviewrs483352914
scholarrs483352914
googlers483352914
pharmgkbrs483352914
gwascentralrs483352914
openSNPrs483352914
23andMers483352914
23andMe allrs483352914
SNP Nexus

SNPshotrs483352914
SNPdbers483352914
MSV3drs483352914
GWAS Ctlgrs483352914
Max Magnitude0
ClinVar
Risk rs483352914(A;A)
Alt rs483352914(A;A)
Reference rs483352914(T;T)
Significance Pathogenic
Disease Reticulate acropigmentation of Kitamura
Variation info
Gene ADAM10
CLNDBN Reticulate acropigmentation of Kitamura
Reversed 1
HGVS NC_000015.9:g.58971378A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074429.3,