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rs727504893

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504893(A;A)
Make rs727504893(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position216418533
GeneUSH2A
is asnp
is mentioned by
dbSNPrs727504893
ebirs727504893
HLIrs727504893
Exacrs727504893
Varsomers727504893
Maprs727504893
PheGenIrs727504893
hapmaprs727504893
1000 genomesrs727504893
hgdprs727504893
ensemblrs727504893
gopubmedrs727504893
geneviewrs727504893
scholarrs727504893
googlers727504893
pharmgkbrs727504893
gwascentralrs727504893
openSNPrs727504893
23andMers727504893
23andMe allrs727504893
SNP Nexus

SNPshotrs727504893
SNPdbers727504893
MSV3drs727504893
GWAS Ctlgrs727504893
Max Magnitude0
ClinVar
Risk rs727504893(A;A)
Alt rs727504893(A;A)
Reference rs727504893(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.216591875C>T
CLNSRC
CLNACC RCV000156272.1,