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rs786205575

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205575(C;T)
Make rs786205575(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position150379406
GeneTCOF1
is asnp
is mentioned by
dbSNPrs786205575
ebirs786205575
HLIrs786205575
Exacrs786205575
Varsomers786205575
Maprs786205575
PheGenIrs786205575
hapmaprs786205575
1000 genomesrs786205575
hgdprs786205575
ensemblrs786205575
gopubmedrs786205575
geneviewrs786205575
scholarrs786205575
googlers786205575
pharmgkbrs786205575
gwascentralrs786205575
openSNPrs786205575
23andMers786205575
23andMe allrs786205575
SNP Nexus

SNPshotrs786205575
SNPdbers786205575
MSV3drs786205575
GWAS Ctlgrs786205575
Max Magnitude0
ClinVar
Risk rs786205575(T;T)
Alt rs786205575(T;T)
Reference rs786205575(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCOF1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.149758969C>T
CLNSRC
CLNACC RCV000171388.1,