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rs200712760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200712760(A;A)
Make rs200712760(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position215888482
GeneUSH2A
is asnp
is mentioned by
dbSNPrs200712760
dbSNP (classic)rs200712760
ClinGenrs200712760
ebirs200712760
HLIrs200712760
Exacrs200712760
Gnomadrs200712760
Varsomers200712760
LitVarrs200712760
Maprs200712760
PheGenIrs200712760
Biobankrs200712760
1000 genomesrs200712760
hgdprs200712760
ensemblrs200712760
geneviewrs200712760
scholarrs200712760
googlers200712760
pharmgkbrs200712760
gwascentralrs200712760
openSNPrs200712760
23andMers200712760
23andMe allrs200712760
SNPshotrs200712760
SNPdbers200712760
MSV3drs200712760
GWAS Ctlgrs200712760
Max Magnitude0
ClinVar
Risk rs200712760(A;A)
Alt rs200712760(A;A)
Reference Rs200712760(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.216061824G>A
CLNSRC
CLNACC RCV000485043.1,