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rs876661247

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661247(C;T)
Make rs876661247(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position127501108
GeneLRSAM1
is asnp
is mentioned by
dbSNPrs876661247
ebirs876661247
HLIrs876661247
Exacrs876661247
Varsomers876661247
Maprs876661247
PheGenIrs876661247
hapmaprs876661247
1000 genomesrs876661247
hgdprs876661247
ensemblrs876661247
gopubmedrs876661247
geneviewrs876661247
scholarrs876661247
googlers876661247
pharmgkbrs876661247
gwascentralrs876661247
openSNPrs876661247
23andMers876661247
23andMe allrs876661247
SNP Nexus

SNPshotrs876661247
SNPdbers876661247
MSV3drs876661247
GWAS Ctlgrs876661247
Max Magnitude0
ClinVar
Risk rs876661247(T;T)
Alt rs876661247(T;T)
Reference rs876661247(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRSAM1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130263387C>T
CLNSRC
CLNACC RCV000214671.1,