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rs786205551

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205551(A;A)
Make rs786205551(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position237493530
GeneMLPH
is asnp
is mentioned by
dbSNPrs786205551
ebirs786205551
HLIrs786205551
Exacrs786205551
Varsomers786205551
Maprs786205551
PheGenIrs786205551
hapmaprs786205551
1000 genomesrs786205551
hgdprs786205551
ensemblrs786205551
gopubmedrs786205551
geneviewrs786205551
scholarrs786205551
googlers786205551
pharmgkbrs786205551
gwascentralrs786205551
openSNPrs786205551
23andMers786205551
23andMe allrs786205551
SNP Nexus

SNPshotrs786205551
SNPdbers786205551
MSV3drs786205551
GWAS Ctlgrs786205551
Max Magnitude0
ClinVar
Risk rs786205551(A;A)
Alt rs786205551(A;A)
Reference rs786205551(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MLPH
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.238402173G>A
CLNSRC
CLNACC RCV000171341.1,