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rs556445621

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs556445621(A;A)
Make rs556445621(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position100989382
GeneC10orf2, MRPL43
is asnp
is mentioned by
dbSNPrs556445621
ebirs556445621
HLIrs556445621
Exacrs556445621
Varsomers556445621
Maprs556445621
PheGenIrs556445621
hapmaprs556445621
1000 genomesrs556445621
hgdprs556445621
ensemblrs556445621
gopubmedrs556445621
geneviewrs556445621
scholarrs556445621
googlers556445621
pharmgkbrs556445621
gwascentralrs556445621
openSNPrs556445621
23andMers556445621
23andMe allrs556445621
SNP Nexus

SNPshotrs556445621
SNPdbers556445621
MSV3drs556445621
GWAS Ctlgrs556445621
Max Magnitude0
ClinVar
Risk rs556445621(A;A)
Alt rs556445621(A;A)
Reference rs556445621(G;G)
Significance Pathogenic
Disease Perrault syndrome 5 not provided
Variation info
Gene MRPL43 C10orf2
CLNDBN Perrault syndrome 5 not provided
Reversed 0
HGVS NC_000010.10:g.102749139G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149470.4, RCV000197750.1,