Have questions? Visit https://www.reddit.com/r/SNPedia

rs752171066

From SNPedia

Orientationplus
Geno Mag Summary
(GAA;GAA) 0 common in clinvar
Make rs752171066(-;-)
Make rs752171066(-;GAA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position8174573
GeneLOC105371520, SNORD118, TMEM107
is asnp
is mentioned by
dbSNPrs752171066
ebirs752171066
HLIrs752171066
Exacrs752171066
Varsomers752171066
Maprs752171066
PheGenIrs752171066
hapmaprs752171066
1000 genomesrs752171066
hgdprs752171066
ensemblrs752171066
gopubmedrs752171066
geneviewrs752171066
scholarrs752171066
googlers752171066
pharmgkbrs752171066
gwascentralrs752171066
openSNPrs752171066
23andMers752171066
23andMe allrs752171066
SNP Nexus

SNPshotrs752171066
SNPdbers752171066
MSV3drs752171066
GWAS Ctlgrs752171066
Max Magnitude0
ClinVar
Risk rs752171066(;)
Alt rs752171066(;)
Reference rs752171066(GAA;GAA)
Significance Pathogenic
Disease Orofaciodigital syndromes
Variation info
Gene TMEM107 SNORD118
CLNDBN Orofaciodigital syndromes
Reversed 0
HGVS NC_000017.10:g.8077891_8077893delGAA
CLNSRC
CLNACC RCV000236136.1,