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rs1057518219

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACAA;ACAA) 0 common in clinvar
Make rs1057518219(-;-)
Make rs1057518219(-;AACA)
Make rs1057518219(AACA;AACA)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position236863
GeneZMYND11
is asnp
is mentioned by
dbSNPrs1057518219
dbSNP (classic)rs1057518219
ClinGenrs1057518219
ebirs1057518219
HLIrs1057518219
Exacrs1057518219
Gnomadrs1057518219
Varsomers1057518219
LitVarrs1057518219
Maprs1057518219
PheGenIrs1057518219
Biobankrs1057518219
1000 genomesrs1057518219
hgdprs1057518219
ensemblrs1057518219
geneviewrs1057518219
scholarrs1057518219
googlers1057518219
pharmgkbrs1057518219
gwascentralrs1057518219
openSNPrs1057518219
23andMers1057518219
23andMe allrs1057518219
SNPshotrs1057518219
SNPdbers1057518219
MSV3drs1057518219
GWAS Ctlgrs1057518219
Max Magnitude0
ClinVar
Risk rs1057518219(-;-)
Alt rs1057518219(-;-)
Reference Rs1057518219(ACAA;ACAA)
Significance Pathogenic
Disease not provided
Variation info
Gene ZMYND11
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.282803_282806delAACA
CLNSRC
CLNACC RCV000413199.1,