rs863223987

Orientation

minus

Stabilized

minus

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

Make rs863223987(ACT;ACT)

Make rs863223987(ACT;GCC)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

241504044

Gene

FH

is a	snp
is	mentioned by
dbSNP	rs863223987
dbSNP (classic)	rs863223987
ClinGen	rs863223987
ebi	rs863223987
HLI	rs863223987
Exac	rs863223987
Gnomad	rs863223987
Varsome	rs863223987
LitVar	rs863223987
Map	rs863223987
PheGenI	rs863223987
Biobank	rs863223987
1000 genomes	rs863223987
hgdp	rs863223987
ensembl	rs863223987
geneview	rs863223987
scholar	rs863223987
google	rs863223987
pharmgkb	rs863223987
gwascentral	rs863223987
openSNP	rs863223987
23andMe	rs863223987
SNPshot	rs863223987
SNPdbe	rs863223987
MSV3d	rs863223987
GWAS Ctlg	rs863223987

Max Magnitude

0

ClinVar
Risk	rs863223987(ACT;ACT)
Alt	rs863223987(ACT;ACT)
Reference	Rs863223987(GCC;GCC)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	FH
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.241667344_241667346delGGCinsAGT
CLNSRC
CLNACC	RCV000198761.2,