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rs786205647

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205647(A;A)
Make rs786205647(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position38506502
GeneLIFR
is asnp
is mentioned by
dbSNPrs786205647
ebirs786205647
HLIrs786205647
Exacrs786205647
Varsomers786205647
Maprs786205647
PheGenIrs786205647
hapmaprs786205647
1000 genomesrs786205647
hgdprs786205647
ensemblrs786205647
gopubmedrs786205647
geneviewrs786205647
scholarrs786205647
googlers786205647
pharmgkbrs786205647
gwascentralrs786205647
openSNPrs786205647
23andMers786205647
23andMe allrs786205647
SNP Nexus

SNPshotrs786205647
SNPdbers786205647
MSV3drs786205647
GWAS Ctlgrs786205647
Max Magnitude0
ClinVar
Risk rs786205647(A;A)
Alt rs786205647(A;A)
Reference rs786205647(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LIFR
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.38506604C>T
CLNSRC
CLNACC RCV000171519.1,