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rs756709134

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756709134(C;T)
Make rs756709134(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position77942606
GeneNEXN
is asnp
is mentioned by
dbSNPrs756709134
ebirs756709134
HLIrs756709134
Exacrs756709134
Varsomers756709134
Maprs756709134
PheGenIrs756709134
hapmaprs756709134
1000 genomesrs756709134
hgdprs756709134
ensemblrs756709134
gopubmedrs756709134
geneviewrs756709134
scholarrs756709134
googlers756709134
pharmgkbrs756709134
gwascentralrs756709134
openSNPrs756709134
23andMers756709134
23andMe allrs756709134
SNP Nexus

SNPshotrs756709134
SNPdbers756709134
MSV3drs756709134
GWAS Ctlgrs756709134
Max Magnitude0
ClinVar
Risk rs756709134(T;T)
Alt rs756709134(T;T)
Reference rs756709134(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene NEXN
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.78408291C>T
CLNSRC
CLNACC RCV000183670.2,