Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052421(-;-)
Make rs796052421(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position52479070
GeneEFHC1
is asnp
is mentioned by
dbSNPrs796052421
dbSNP (classic)rs796052421
ClinGenrs796052421
ebirs796052421
HLIrs796052421
Exacrs796052421
Gnomadrs796052421
Varsomers796052421
LitVarrs796052421
Maprs796052421
PheGenIrs796052421
Biobankrs796052421
1000 genomesrs796052421
hgdprs796052421
ensemblrs796052421
geneviewrs796052421
scholarrs796052421
googlers796052421
pharmgkbrs796052421
gwascentralrs796052421
openSNPrs796052421
23andMers796052421
SNPshotrs796052421
SNPdbers796052421
MSV3drs796052421
GWAS Ctlgrs796052421
Max Magnitude0
ClinVar
Risk rs796052421(-;-)
Alt rs796052421(-;-)
Reference Rs796052421(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene EFHC1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.52343868delT
CLNSRC
CLNACC RCV000187378.1,