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rs1057518121

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518121(C;T)
Make rs1057518121(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position248345
GeneLOC107984190, ZMYND11
is asnp
is mentioned by
dbSNPrs1057518121
dbSNP (old)rs1057518121
ClinGenrs1057518121
ebirs1057518121
HLIrs1057518121
Exacrs1057518121
Gnomadrs1057518121
Varsomers1057518121
Maprs1057518121
PheGenIrs1057518121
Biobankrs1057518121
1000 genomesrs1057518121
hgdprs1057518121
ensemblrs1057518121
gopubmedrs1057518121
geneviewrs1057518121
scholarrs1057518121
googlers1057518121
pharmgkbrs1057518121
gwascentralrs1057518121
openSNPrs1057518121
23andMers1057518121
23andMe allrs1057518121
SNPshotrs1057518121
SNPdbers1057518121
MSV3drs1057518121
GWAS Ctlgrs1057518121
Max Magnitude0
ClinVar
Risk rs1057518121(T;T)
Alt rs1057518121(T;T)
Reference Rs1057518121(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZMYND11
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.294285C>T
CLNSRC
CLNACC RCV000413358.1,