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rs727505170

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505170(A;A)
Make rs727505170(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position215680168
GeneUSH2A
is asnp
is mentioned by
dbSNPrs727505170
ebirs727505170
HLIrs727505170
Exacrs727505170
Varsomers727505170
Maprs727505170
PheGenIrs727505170
hapmaprs727505170
1000 genomesrs727505170
hgdprs727505170
ensemblrs727505170
gopubmedrs727505170
geneviewrs727505170
scholarrs727505170
googlers727505170
pharmgkbrs727505170
gwascentralrs727505170
openSNPrs727505170
23andMers727505170
23andMe allrs727505170
SNP Nexus

SNPshotrs727505170
SNPdbers727505170
MSV3drs727505170
GWAS Ctlgrs727505170
Max Magnitude0
ClinVar
Risk rs727505170(A;A)
Alt rs727505170(A;A)
Reference rs727505170(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene USH2A
CLNDBN not specified not provided
Reversed 1
HGVS NC_000001.10:g.215853510C>T
CLNSRC
CLNACC RCV000156650.2, RCV000171167.1,