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rs752317877

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752317877(C;T)
Make rs752317877(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position26212590
GeneHADHA
is asnp
is mentioned by
dbSNPrs752317877
ebirs752317877
HLIrs752317877
Exacrs752317877
Varsomers752317877
Maprs752317877
PheGenIrs752317877
hapmaprs752317877
1000 genomesrs752317877
hgdprs752317877
ensemblrs752317877
gopubmedrs752317877
geneviewrs752317877
scholarrs752317877
googlers752317877
pharmgkbrs752317877
gwascentralrs752317877
openSNPrs752317877
23andMers752317877
23andMe allrs752317877
SNP Nexus

SNPshotrs752317877
SNPdbers752317877
MSV3drs752317877
GWAS Ctlgrs752317877
Max Magnitude0
ClinVar
Risk rs752317877(T;T)
Alt rs752317877(T;T)
Reference rs752317877(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HADHA
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.26435459C>T
CLNSRC
CLNACC RCV000185931.1,