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rs200111698

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200111698(C;T)
Make rs200111698(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position158706278
GeneETFDH
is asnp
is mentioned by
dbSNPrs200111698
ebirs200111698
HLIrs200111698
Exacrs200111698
Varsomers200111698
Maprs200111698
PheGenIrs200111698
hapmaprs200111698
1000 genomesrs200111698
hgdprs200111698
ensemblrs200111698
gopubmedrs200111698
geneviewrs200111698
scholarrs200111698
googlers200111698
pharmgkbrs200111698
gwascentralrs200111698
openSNPrs200111698
23andMers200111698
23andMe allrs200111698
SNP Nexus

SNPshotrs200111698
SNPdbers200111698
MSV3drs200111698
GWAS Ctlgrs200111698
Max Magnitude0
ClinVar
Risk rs200111698(T;T)
Alt rs200111698(T;T)
Reference rs200111698(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ETFDH
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.159627430C>T
CLNSRC
CLNACC RCV000185900.1,