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rs756981921

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs756981921(A;C)
Make rs756981921(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position193642808
GeneOPA1
is asnp
is mentioned by
dbSNPrs756981921
ebirs756981921
HLIrs756981921
Exacrs756981921
Varsomers756981921
Maprs756981921
PheGenIrs756981921
hapmaprs756981921
1000 genomesrs756981921
hgdprs756981921
ensemblrs756981921
gopubmedrs756981921
geneviewrs756981921
scholarrs756981921
googlers756981921
pharmgkbrs756981921
gwascentralrs756981921
openSNPrs756981921
23andMers756981921
23andMe allrs756981921
SNP Nexus

SNPshotrs756981921
SNPdbers756981921
MSV3drs756981921
GWAS Ctlgrs756981921
Max Magnitude0
ClinVar
Risk rs756981921(C;C)
Alt rs756981921(C;C)
Reference rs756981921(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OPA1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.193360597A>C
CLNSRC
CLNACC RCV000197106.1,