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rs201757275

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201757275(C;C)
Make rs201757275(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position45954395
GeneEPG5
is asnp
is mentioned by
dbSNPrs201757275
ebirs201757275
HLIrs201757275
Exacrs201757275
Varsomers201757275
Maprs201757275
PheGenIrs201757275
hapmaprs201757275
1000 genomesrs201757275
hgdprs201757275
ensemblrs201757275
gopubmedrs201757275
geneviewrs201757275
scholarrs201757275
googlers201757275
pharmgkbrs201757275
gwascentralrs201757275
openSNPrs201757275
23andMers201757275
23andMe allrs201757275
SNP Nexus

SNPshotrs201757275
SNPdbers201757275
MSV3drs201757275
GWAS Ctlgrs201757275
Max Magnitude0
ClinVar
Risk rs201757275(C;C)
Alt rs201757275(C;C)
Reference rs201757275(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EPG5
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.43534361T>C
CLNSRC
CLNACC RCV000172928.1,