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rs727504608

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727504608(A;A)
Make rs727504608(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position215759746
GeneUSH2A
is asnp
is mentioned by
dbSNPrs727504608
ebirs727504608
HLIrs727504608
Exacrs727504608
Varsomers727504608
Maprs727504608
PheGenIrs727504608
hapmaprs727504608
1000 genomesrs727504608
hgdprs727504608
ensemblrs727504608
gopubmedrs727504608
geneviewrs727504608
scholarrs727504608
googlers727504608
pharmgkbrs727504608
gwascentralrs727504608
openSNPrs727504608
23andMers727504608
23andMe allrs727504608
SNP Nexus

SNPshotrs727504608
SNPdbers727504608
MSV3drs727504608
GWAS Ctlgrs727504608
Max Magnitude0
ClinVar
Risk rs727504608(A;A)
Alt rs727504608(A;A)
Reference rs727504608(T;T)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.215933088A>T
CLNSRC
CLNACC RCV000155859.1,