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rs397509395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509395(A;A)
Make rs397509395(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position109727130
GeneFIG4
is asnp
is mentioned by
dbSNPrs397509395
ebirs397509395
HLIrs397509395
Exacrs397509395
Varsomers397509395
Maprs397509395
PheGenIrs397509395
hapmaprs397509395
1000 genomesrs397509395
hgdprs397509395
ensemblrs397509395
gopubmedrs397509395
geneviewrs397509395
scholarrs397509395
googlers397509395
pharmgkbrs397509395
gwascentralrs397509395
openSNPrs397509395
23andMers397509395
23andMe allrs397509395
SNP Nexus

SNPshotrs397509395
SNPdbers397509395
MSV3drs397509395
GWAS Ctlgrs397509395
Max Magnitude0
ClinVar
Risk rs397509395(A;A)
Alt rs397509395(A;A)
Reference rs397509395(G;G)
Significance Pathogenic
Disease Yunis Varon syndrome
Variation info
Gene FIG4
CLNDBN Yunis Varon syndrome
Reversed 0
HGVS NC_000006.11:g.110048333G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043690.3,