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rs796051941

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051941(C;T)
Make rs796051941(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position15645331
GeneBTD
is asnp
is mentioned by
dbSNPrs796051941
ebirs796051941
HLIrs796051941
Exacrs796051941
Varsomers796051941
Maprs796051941
PheGenIrs796051941
hapmaprs796051941
1000 genomesrs796051941
hgdprs796051941
ensemblrs796051941
gopubmedrs796051941
geneviewrs796051941
scholarrs796051941
googlers796051941
pharmgkbrs796051941
gwascentralrs796051941
openSNPrs796051941
23andMers796051941
23andMe allrs796051941
SNP Nexus

SNPshotrs796051941
SNPdbers796051941
MSV3drs796051941
GWAS Ctlgrs796051941
Max Magnitude0
ClinVar
Risk rs796051941(T;T)
Alt rs796051941(T;T)
Reference rs796051941(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BTD
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.15686838C>T
CLNSRC
CLNACC RCV000185808.1,