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rs1057521717

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521717(G;G)
Make rs1057521717(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position88730243
GeneMEF2C
is asnp
is mentioned by
dbSNPrs1057521717
dbSNP (classic)rs1057521717
ClinGenrs1057521717
ebirs1057521717
HLIrs1057521717
Exacrs1057521717
Gnomadrs1057521717
Varsomers1057521717
LitVarrs1057521717
Maprs1057521717
PheGenIrs1057521717
Biobankrs1057521717
1000 genomesrs1057521717
hgdprs1057521717
ensemblrs1057521717
geneviewrs1057521717
scholarrs1057521717
googlers1057521717
pharmgkbrs1057521717
gwascentralrs1057521717
openSNPrs1057521717
23andMers1057521717
23andMe allrs1057521717
SNPshotrs1057521717
SNPdbers1057521717
MSV3drs1057521717
GWAS Ctlgrs1057521717
Max Magnitude0
ClinVar
Risk rs1057521717(G;G)
Alt rs1057521717(G;G)
Reference Rs1057521717(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEF2C
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.88026060A>C
CLNSRC
CLNACC RCV000423248.1,