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rs483352915

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs483352915(-;-)
Make rs483352915(-;A)
ReferenceGRCh38 38.1/142
Chromosome15
Position58627796
GeneADAM10
is asnp
is mentioned by
dbSNPrs483352915
dbSNP (classic)rs483352915
ClinGenrs483352915
ebirs483352915
HLIrs483352915
Exacrs483352915
Gnomadrs483352915
Varsomers483352915
LitVarrs483352915
Maprs483352915
PheGenIrs483352915
Biobankrs483352915
1000 genomesrs483352915
hgdprs483352915
ensemblrs483352915
geneviewrs483352915
scholarrs483352915
googlers483352915
pharmgkbrs483352915
gwascentralrs483352915
openSNPrs483352915
23andMers483352915
SNPshotrs483352915
SNPdbers483352915
MSV3drs483352915
GWAS Ctlgrs483352915
Max Magnitude0
ClinVar
Risk rs483352915(-;-)
Alt rs483352915(-;-)
Reference Rs483352915(A;A)
Significance Pathogenic
Disease Reticulate acropigmentation of Kitamura
Variation info
Gene ADAM10
CLNDBN Reticulate acropigmentation of Kitamura
Reversed 1
HGVS NC_000015.9:g.58919995delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000074430.3,