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rs13407355

From SNPedia

Orientationplus
Make rs13407355(C;C)
Make rs13407355(C;G)
Make rs13407355(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position71513823
GeneDYSF
is asnp
is mentioned by
dbSNPrs13407355
ebirs13407355
HLIrs13407355
Exacrs13407355
Varsomers13407355
Maprs13407355
PheGenIrs13407355
hapmaprs13407355
1000 genomesrs13407355
hgdprs13407355
ensemblrs13407355
gopubmedrs13407355
geneviewrs13407355
scholarrs13407355
googlers13407355
pharmgkbrs13407355
gwascentralrs13407355
openSNPrs13407355
23andMers13407355
23andMe allrs13407355
SNP Nexus

SNPshotrs13407355
SNPdbers13407355
MSV3drs13407355
GWAS Ctlgrs13407355
Max Magnitude
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs13407355(A,G;A,G)
Alt rs13407355(A,G;A,G)
Reference rs13407355(C;C)
Significance Other
Disease not specified
Variation info
Gene DYSF
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.71740953C>G
CLNSRC HGMD
CLNACC RCV000080309.7,