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rs796051975

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051975(A;A)
Make rs796051975(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position26279134
GeneHADHB
is asnp
is mentioned by
dbSNPrs796051975
ebirs796051975
HLIrs796051975
Exacrs796051975
Varsomers796051975
Maprs796051975
PheGenIrs796051975
hapmaprs796051975
1000 genomesrs796051975
hgdprs796051975
ensemblrs796051975
gopubmedrs796051975
geneviewrs796051975
scholarrs796051975
googlers796051975
pharmgkbrs796051975
gwascentralrs796051975
openSNPrs796051975
23andMers796051975
23andMe allrs796051975
SNP Nexus

SNPshotrs796051975
SNPdbers796051975
MSV3drs796051975
GWAS Ctlgrs796051975
Max Magnitude0
ClinVar
Risk rs796051975(A;A)
Alt rs796051975(A;A)
Reference rs796051975(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene HADHB
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.26502002G>A
CLNSRC
CLNACC RCV000185944.1,