rs397509395

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs397509395(A;A)

Make rs397509395(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

109727130

Gene

FIG4

is a	snp
is	mentioned by
dbSNP	rs397509395
dbSNP (classic)	rs397509395
ClinGen	rs397509395
ebi	rs397509395
HLI	rs397509395
Exac	rs397509395
Gnomad	rs397509395
Varsome	rs397509395
LitVar	rs397509395
Map	rs397509395
PheGenI	rs397509395
Biobank	rs397509395
1000 genomes	rs397509395
hgdp	rs397509395
ensembl	rs397509395
geneview	rs397509395
scholar	rs397509395
google	rs397509395
pharmgkb	rs397509395
gwascentral	rs397509395
openSNP	rs397509395
23andMe	rs397509395
SNPshot	rs397509395
SNPdbe	rs397509395
MSV3d	rs397509395
GWAS Ctlg	rs397509395

Max Magnitude

0

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 UniProtKB (protein)
CLNACC	RCV000043690.4,