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rs765086319

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765086319(A;A)
Make rs765086319(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position74726273
GeneFA2H
is asnp
is mentioned by
dbSNPrs765086319
ebirs765086319
HLIrs765086319
Exacrs765086319
Varsomers765086319
Maprs765086319
PheGenIrs765086319
hapmaprs765086319
1000 genomesrs765086319
hgdprs765086319
ensemblrs765086319
gopubmedrs765086319
geneviewrs765086319
scholarrs765086319
googlers765086319
pharmgkbrs765086319
gwascentralrs765086319
openSNPrs765086319
23andMers765086319
23andMe allrs765086319
SNP Nexus

SNPshotrs765086319
SNPdbers765086319
MSV3drs765086319
GWAS Ctlgrs765086319
Max Magnitude0
ClinVar
Risk rs765086319(A;A)
Alt rs765086319(A;A)
Reference rs765086319(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene FA2H
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000016.9:g.74760171G>A
CLNSRC
CLNACC RCV000190745.1,