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rs796051974

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051974(-;-)
Make rs796051974(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position26283049
GeneHADHB
is asnp
is mentioned by
dbSNPrs796051974
ebirs796051974
HLIrs796051974
Exacrs796051974
Varsomers796051974
Maprs796051974
PheGenIrs796051974
hapmaprs796051974
1000 genomesrs796051974
hgdprs796051974
ensemblrs796051974
gopubmedrs796051974
geneviewrs796051974
scholarrs796051974
googlers796051974
pharmgkbrs796051974
gwascentralrs796051974
openSNPrs796051974
23andMers796051974
23andMe allrs796051974
SNP Nexus

SNPshotrs796051974
SNPdbers796051974
MSV3drs796051974
GWAS Ctlgrs796051974
Max Magnitude0
ClinVar
Risk rs796051974(;)
Alt rs796051974(;)
Reference rs796051974(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene HADHB
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.26505917delT
CLNSRC
CLNACC RCV000185943.1,