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rs754277797

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754277797(C;C)
Make rs754277797(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position855770
GeneELANE
is asnp
is mentioned by
dbSNPrs754277797
ebirs754277797
HLIrs754277797
Exacrs754277797
Varsomers754277797
Maprs754277797
PheGenIrs754277797
hapmaprs754277797
1000 genomesrs754277797
hgdprs754277797
ensemblrs754277797
gopubmedrs754277797
geneviewrs754277797
scholarrs754277797
googlers754277797
pharmgkbrs754277797
gwascentralrs754277797
openSNPrs754277797
23andMers754277797
23andMe allrs754277797
SNP Nexus

SNPshotrs754277797
SNPdbers754277797
MSV3drs754277797
GWAS Ctlgrs754277797
Max Magnitude0
ClinVar
Risk rs754277797(C;C)
Alt rs754277797(C;C)
Reference rs754277797(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ELANE
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.855770G>C
CLNSRC
CLNACC RCV000232592.1,