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rs786200981

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200981(-;-)
Make rs786200981(-;G)
Make rs786200981(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position88729255
GeneMEF2C
is asnp
is mentioned by
dbSNPrs786200981
ebirs786200981
HLIrs786200981
Exacrs786200981
Varsomers786200981
Maprs786200981
PheGenIrs786200981
hapmaprs786200981
1000 genomesrs786200981
hgdprs786200981
ensemblrs786200981
gopubmedrs786200981
geneviewrs786200981
scholarrs786200981
googlers786200981
pharmgkbrs786200981
gwascentralrs786200981
openSNPrs786200981
23andMers786200981
23andMe allrs786200981
SNP Nexus

SNPshotrs786200981
SNPdbers786200981
MSV3drs786200981
GWAS Ctlgrs786200981
Max Magnitude0
ClinVar
Risk rs786200981(G;G)
Alt rs786200981(G;G)
Reference rs786200981(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MEF2C
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.88025073dupC
CLNSRC
CLNACC RCV000153485.2,