rs786200937

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GTAAATTT;GTAAATTT)	0	common in clinvar
(I;I)	0	common genotype
(TAAATTTG;TAAATTTG)	0	common in clinvar

Make rs786200937(-;-)

Make rs786200937(-;TAAATTTG)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

109741499

Gene

FIG4

is a	snp
is	mentioned by
dbSNP	rs786200937
dbSNP (classic)	rs786200937
ClinGen	rs786200937
ebi	rs786200937
HLI	rs786200937
Exac	rs786200937
Gnomad	rs786200937
Varsome	rs786200937
LitVar	rs786200937
Map	rs786200937
PheGenI	rs786200937
Biobank	rs786200937
1000 genomes	rs786200937
hgdp	rs786200937
ensembl	rs786200937
geneview	rs786200937
scholar	rs786200937
google	rs786200937
pharmgkb	rs786200937
gwascentral	rs786200937
openSNP	rs786200937
23andMe	rs786200937
SNPshot	rs786200937
SNPdbe	rs786200937
MSV3d	rs786200937
GWAS Ctlg	rs786200937

Max Magnitude

0

ClinVar
Risk	rs786200937(-;-) Rs786200937(GTAAATTT;GTAAATTT)
Alt	rs786200937(-;-) Rs786200937(GTAAATTT;GTAAATTT)
Reference	Rs786200937(TAAATTTG;TAAATTTG)
Significance	Pathogenic
Disease	Yunis Varon syndrome not provided
Variation	info
Gene	FIG4
CLNDBN	Yunis Varon syndrome not provided
Reversed	0
HGVS	NC_000006.11:g.110062702_110062709delTAAATTTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043691.4, RCV000236453.2,