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rs397509394

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs397509394(-;-)
Make rs397509394(-;GT)
ReferenceGRCh38 38.1/141
Chromosome6
Position109760372
GeneFIG4
is asnp
is mentioned by
dbSNPrs397509394
ebirs397509394
HLIrs397509394
Exacrs397509394
Varsomers397509394
Maprs397509394
PheGenIrs397509394
hapmaprs397509394
1000 genomesrs397509394
hgdprs397509394
ensemblrs397509394
gopubmedrs397509394
geneviewrs397509394
scholarrs397509394
googlers397509394
pharmgkbrs397509394
gwascentralrs397509394
openSNPrs397509394
23andMers397509394
23andMe allrs397509394
SNP Nexus

SNPshotrs397509394
SNPdbers397509394
MSV3drs397509394
GWAS Ctlgrs397509394
Max Magnitude0
ClinVar
Risk rs397509394(;)
Alt rs397509394(;)
Reference rs397509394(GT;GT)
Significance Pathogenic
Disease Yunis Varon syndrome
Variation info
Gene FIG4
CLNDBN Yunis Varon syndrome
Reversed 0
HGVS NC_000006.11:g.110081575_110081576delGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000043689.4,