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rs200777054

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200777054(G;T)
Make rs200777054(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position26269952
GeneHADHB
is asnp
is mentioned by
dbSNPrs200777054
dbSNP (old)rs200777054
ClinGenrs200777054
ebirs200777054
HLIrs200777054
Exacrs200777054
Gnomadrs200777054
Varsomers200777054
Maprs200777054
PheGenIrs200777054
Biobankrs200777054
1000 genomesrs200777054
hgdprs200777054
ensemblrs200777054
gopubmedrs200777054
geneviewrs200777054
scholarrs200777054
googlers200777054
pharmgkbrs200777054
gwascentralrs200777054
openSNPrs200777054
23andMers200777054
23andMe allrs200777054
SNPshotrs200777054
SNPdbers200777054
MSV3drs200777054
GWAS Ctlgrs200777054
Max Magnitude0
ClinVar
Risk rs200777054(C;C) rs200777054(T;T)
Alt rs200777054(C;C) rs200777054(T;T)
Reference Rs200777054(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HADHB
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.26492820G>C; NC_000002.11:g.26492820G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000239550.1, RCV000483833.1,