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rs1057520533

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520533(C;T)
Make rs1057520533(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position15644722
GeneBTD
is asnp
is mentioned by
dbSNPrs1057520533
dbSNP (old)rs1057520533
ClinGenrs1057520533
ebirs1057520533
HLIrs1057520533
Exacrs1057520533
Gnomadrs1057520533
Varsomers1057520533
Maprs1057520533
PheGenIrs1057520533
Biobankrs1057520533
1000 genomesrs1057520533
hgdprs1057520533
ensemblrs1057520533
gopubmedrs1057520533
geneviewrs1057520533
scholarrs1057520533
googlers1057520533
pharmgkbrs1057520533
gwascentralrs1057520533
openSNPrs1057520533
23andMers1057520533
23andMe allrs1057520533
SNPshotrs1057520533
SNPdbers1057520533
MSV3drs1057520533
GWAS Ctlgrs1057520533
Max Magnitude0
ClinVar
Risk rs1057520533(T;T)
Alt rs1057520533(T;T)
Reference Rs1057520533(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BTD
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.15686229C>T
CLNSRC
CLNACC RCV000428786.1,