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rs727503918

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503918(C;C)
Make rs727503918(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position76311387
GeneETFA
is asnp
is mentioned by
dbSNPrs727503918
ebirs727503918
HLIrs727503918
Exacrs727503918
Varsomers727503918
Maprs727503918
PheGenIrs727503918
hapmaprs727503918
1000 genomesrs727503918
hgdprs727503918
ensemblrs727503918
gopubmedrs727503918
geneviewrs727503918
scholarrs727503918
googlers727503918
pharmgkbrs727503918
gwascentralrs727503918
openSNPrs727503918
23andMers727503918
23andMe allrs727503918
SNP Nexus

SNPshotrs727503918
SNPdbers727503918
MSV3drs727503918
GWAS Ctlgrs727503918
Max Magnitude0
ClinVar
Risk rs727503918(C;C)
Alt rs727503918(C;C)
Reference rs727503918(T;T)
Significance Other
Disease not provided
Variation info
Gene ETFA
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.76603728A>G
CLNSRC
CLNACC RCV000153198.4,