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rs727503873

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503873(A;G)
Make rs727503873(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position77280082
GenePOMT2
is asnp
is mentioned by
dbSNPrs727503873
ebirs727503873
HLIrs727503873
Exacrs727503873
Varsomers727503873
Maprs727503873
PheGenIrs727503873
hapmaprs727503873
1000 genomesrs727503873
hgdprs727503873
ensemblrs727503873
gopubmedrs727503873
geneviewrs727503873
scholarrs727503873
googlers727503873
pharmgkbrs727503873
gwascentralrs727503873
openSNPrs727503873
23andMers727503873
23andMe allrs727503873
SNP Nexus

SNPshotrs727503873
SNPdbers727503873
MSV3drs727503873
GWAS Ctlgrs727503873
Max Magnitude0
ClinVar
Risk rs727503873(G;G)
Alt rs727503873(G;G)
Reference rs727503873(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene POMT2
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.77746425T>C
CLNSRC
CLNACC RCV000153052.3,