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rs786205457

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205457(C;T)
Make rs786205457(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position68142972
GeneMYPN
is asnp
is mentioned by
dbSNPrs786205457
ebirs786205457
HLIrs786205457
Exacrs786205457
Varsomers786205457
Maprs786205457
PheGenIrs786205457
hapmaprs786205457
1000 genomesrs786205457
hgdprs786205457
ensemblrs786205457
gopubmedrs786205457
geneviewrs786205457
scholarrs786205457
googlers786205457
pharmgkbrs786205457
gwascentralrs786205457
openSNPrs786205457
23andMers786205457
23andMe allrs786205457
SNP Nexus

SNPshotrs786205457
SNPdbers786205457
MSV3drs786205457
GWAS Ctlgrs786205457
Max Magnitude0
ClinVar
Risk rs786205457(T;T)
Alt rs786205457(T;T)
Reference rs786205457(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYPN
CLNDBN not provided not specified
Reversed 0
HGVS NC_000010.10:g.69902729C>T
CLNSRC
CLNACC RCV000171175.1, RCV000220380.1,