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rs1057521648

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521648(C;T)
Make rs1057521648(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127818341
GeneENG, LOC102723566
is asnp
is mentioned by
dbSNPrs1057521648
dbSNP (old)rs1057521648
ClinGenrs1057521648
ebirs1057521648
HLIrs1057521648
Exacrs1057521648
Gnomadrs1057521648
Varsomers1057521648
Maprs1057521648
PheGenIrs1057521648
Biobankrs1057521648
1000 genomesrs1057521648
hgdprs1057521648
ensemblrs1057521648
gopubmedrs1057521648
geneviewrs1057521648
scholarrs1057521648
googlers1057521648
pharmgkbrs1057521648
gwascentralrs1057521648
openSNPrs1057521648
23andMers1057521648
23andMe allrs1057521648
SNPshotrs1057521648
SNPdbers1057521648
MSV3drs1057521648
GWAS Ctlgrs1057521648
Max Magnitude0
ClinVar
Risk rs1057521648(T;T)
Alt rs1057521648(T;T)
Reference Rs1057521648(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ENG LOC102723566
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130580620G>A
CLNSRC
CLNACC RCV000421678.1,