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rs199763682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199763682(A;A)
Make rs199763682(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position76285676
GeneETFA
is asnp
is mentioned by
dbSNPrs199763682
dbSNP (old)rs199763682
ClinGenrs199763682
ebirs199763682
HLIrs199763682
Exacrs199763682
Gnomadrs199763682
Varsomers199763682
LitVarrs199763682
Maprs199763682
PheGenIrs199763682
Biobankrs199763682
1000 genomesrs199763682
hgdprs199763682
ensemblrs199763682
gopubmedrs199763682
geneviewrs199763682
scholarrs199763682
googlers199763682
pharmgkbrs199763682
gwascentralrs199763682
openSNPrs199763682
23andMers199763682
23andMe allrs199763682
SNPshotrs199763682
SNPdbers199763682
MSV3drs199763682
GWAS Ctlgrs199763682
Max Magnitude0
ClinVar
Risk rs199763682(A;A)
Alt rs199763682(A;A)
Reference Rs199763682(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ETFA
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.76578017G>A
CLNSRC
CLNACC RCV000254926.1,