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rs786205443

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205443(A;A)
Make rs786205443(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42755539
GeneP3H1
is asnp
is mentioned by
dbSNPrs786205443
ebirs786205443
HLIrs786205443
Exacrs786205443
Varsomers786205443
Maprs786205443
PheGenIrs786205443
hapmaprs786205443
1000 genomesrs786205443
hgdprs786205443
ensemblrs786205443
gopubmedrs786205443
geneviewrs786205443
scholarrs786205443
googlers786205443
pharmgkbrs786205443
gwascentralrs786205443
openSNPrs786205443
23andMers786205443
23andMe allrs786205443
SNP Nexus

SNPshotrs786205443
SNPdbers786205443
MSV3drs786205443
GWAS Ctlgrs786205443
Max Magnitude0
ClinVar
Risk rs786205443(A;A)
Alt rs786205443(A;A)
Reference rs786205443(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LEPRE1 P3H1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43221210C>T
CLNSRC
CLNACC RCV000171152.1,