rs398124538

Orientation

minus

Stabilized

minus

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

Make rs398124538(GC;TA)

Make rs398124538(TA;TA)

Reference

GRCh38 38.1/141

Chromosome

17

Position

17223929

Gene

FLCN

is a	snp
is	mentioned by
dbSNP	rs398124538
dbSNP (classic)	rs398124538
ClinGen	rs398124538
ebi	rs398124538
HLI	rs398124538
Exac	rs398124538
Gnomad	rs398124538
Varsome	rs398124538
LitVar	rs398124538
Map	rs398124538
PheGenI	rs398124538
Biobank	rs398124538
1000 genomes	rs398124538
hgdp	rs398124538
ensembl	rs398124538
geneview	rs398124538
scholar	rs398124538
google	rs398124538
pharmgkb	rs398124538
gwascentral	rs398124538
openSNP	rs398124538
23andMe	rs398124538
SNPshot	rs398124538
SNPdbe	rs398124538
MSV3d	rs398124538
GWAS Ctlg	rs398124538

Max Magnitude

0

ClinVar
Risk	rs398124538(TA;TA)
Alt	rs398124538(TA;TA)
Reference	Rs398124538(GC;GC)
Significance	Pathogenic
Disease	not provided Multiple fibrofolliculomas
Variation	info
Gene	FLCN
CLNDBN	not provided Multiple fibrofolliculomas
Reversed	1
HGVS	NC_000017.10:g.17127243_17127244delGCinsTA
CLNSRC	HGMD
CLNACC	RCV000082640.4, RCV000133394.3,