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rs786205641

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205641(-;-)
Make rs786205641(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position237527482
GeneMLPH
is asnp
is mentioned by
dbSNPrs786205641
ebirs786205641
HLIrs786205641
Exacrs786205641
Varsomers786205641
Maprs786205641
PheGenIrs786205641
hapmaprs786205641
1000 genomesrs786205641
hgdprs786205641
ensemblrs786205641
gopubmedrs786205641
geneviewrs786205641
scholarrs786205641
googlers786205641
pharmgkbrs786205641
gwascentralrs786205641
openSNPrs786205641
23andMers786205641
23andMe allrs786205641
SNP Nexus

SNPshotrs786205641
SNPdbers786205641
MSV3drs786205641
GWAS Ctlgrs786205641
Max Magnitude0
ClinVar
Risk rs786205641(;)
Alt rs786205641(;)
Reference rs786205641(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MLPH
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.238436125delC
CLNSRC
CLNACC RCV000171507.1,