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rs797044873

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044873(G;T)
Make rs797044873(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position10284751
GeneSNAP25
is asnp
is mentioned by
dbSNPrs797044873
ebirs797044873
HLIrs797044873
Exacrs797044873
Varsomers797044873
Maprs797044873
PheGenIrs797044873
hapmaprs797044873
1000 genomesrs797044873
hgdprs797044873
ensemblrs797044873
gopubmedrs797044873
geneviewrs797044873
scholarrs797044873
googlers797044873
pharmgkbrs797044873
gwascentralrs797044873
openSNPrs797044873
23andMers797044873
23andMe allrs797044873
SNP Nexus

SNPshotrs797044873
SNPdbers797044873
MSV3drs797044873
GWAS Ctlgrs797044873
Max Magnitude0
ClinVar
Risk rs797044873(T;T)
Alt rs797044873(T;T)
Reference rs797044873(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SNAP25
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000020.10:g.10265399G>T
CLNSRC
CLNACC RCV000190683.1,