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rs786205562

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205562(G;T)
Make rs786205562(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position49121728
GeneLAMB2, USP19
is asnp
is mentioned by
dbSNPrs786205562
ebirs786205562
HLIrs786205562
Exacrs786205562
Varsomers786205562
Maprs786205562
PheGenIrs786205562
hapmaprs786205562
1000 genomesrs786205562
hgdprs786205562
ensemblrs786205562
gopubmedrs786205562
geneviewrs786205562
scholarrs786205562
googlers786205562
pharmgkbrs786205562
gwascentralrs786205562
openSNPrs786205562
23andMers786205562
23andMe allrs786205562
SNP Nexus

SNPshotrs786205562
SNPdbers786205562
MSV3drs786205562
GWAS Ctlgrs786205562
Max Magnitude0
ClinVar
Risk rs786205562(T;T)
Alt rs786205562(T;T)
Reference rs786205562(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMB2 USP19
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.49159161C>A
CLNSRC
CLNACC RCV000171362.1,