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rs771053807

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs771053807(-;-)
Make rs771053807(-;CAGTTC)
Make rs771053807(CAGTTC;CAGTTC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position63483870
GeneACE
is asnp
is mentioned by
dbSNPrs771053807
ebirs771053807
HLIrs771053807
Exacrs771053807
Varsomers771053807
Maprs771053807
PheGenIrs771053807
hapmaprs771053807
1000 genomesrs771053807
hgdprs771053807
ensemblrs771053807
gopubmedrs771053807
geneviewrs771053807
scholarrs771053807
googlers771053807
pharmgkbrs771053807
gwascentralrs771053807
openSNPrs771053807
23andMers771053807
23andMe allrs771053807
SNP Nexus

SNPshotrs771053807
SNPdbers771053807
MSV3drs771053807
GWAS Ctlgrs771053807
Max Magnitude0
ClinVar
Risk rs771053807(CAGTTC;CAGTTC)
Alt rs771053807(CAGTTC;CAGTTC)
Reference rs771053807(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACE
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.61561231_61561232insCAGTTC
CLNSRC
CLNACC RCV000224410.1,