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rs1057520552

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520552(G;T)
Make rs1057520552(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position152154894
GeneSYNE1
is asnp
is mentioned by
dbSNPrs1057520552
dbSNP (old)rs1057520552
ClinGenrs1057520552
ebirs1057520552
HLIrs1057520552
Exacrs1057520552
Gnomadrs1057520552
Varsomers1057520552
Maprs1057520552
PheGenIrs1057520552
Biobankrs1057520552
1000 genomesrs1057520552
hgdprs1057520552
ensemblrs1057520552
gopubmedrs1057520552
geneviewrs1057520552
scholarrs1057520552
googlers1057520552
pharmgkbrs1057520552
gwascentralrs1057520552
openSNPrs1057520552
23andMers1057520552
23andMe allrs1057520552
SNPshotrs1057520552
SNPdbers1057520552
MSV3drs1057520552
GWAS Ctlgrs1057520552
Max Magnitude0
ClinVar
Risk rs1057520552(T;T)
Alt rs1057520552(T;T)
Reference Rs1057520552(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SYNE1
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.152476029C>A
CLNSRC
CLNACC RCV000430890.1,