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rs776256380

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776256380(A;A)
Make rs776256380(A;G)
ReferenceGRCh38.p7 38.3/149
ChromosomeX
Position85958965
GeneCHM
is asnp
is mentioned by
dbSNPrs776256380
dbSNP (old)rs776256380
ClinGenrs776256380
ebirs776256380
HLIrs776256380
Exacrs776256380
Gnomadrs776256380
Varsomers776256380
Maprs776256380
PheGenIrs776256380
Biobankrs776256380
1000 genomesrs776256380
hgdprs776256380
ensemblrs776256380
gopubmedrs776256380
geneviewrs776256380
scholarrs776256380
googlers776256380
pharmgkbrs776256380
gwascentralrs776256380
openSNPrs776256380
23andMers776256380
23andMe allrs776256380
SNPshotrs776256380
SNPdbers776256380
MSV3drs776256380
GWAS Ctlgrs776256380
Max Magnitude0
ClinVar
Risk rs776256380(A;A)
Alt rs776256380(A;A)
Reference Rs776256380(G;G)
Significance Pathogenic
Disease Choroideremia
Variation info
Gene CHM
CLNDBN Choroideremia
Reversed 0
HGVS NC_000023.10:g.85213970G>A
CLNSRC
CLNACC RCV000302207.1,