rs121908898

Orientation

plus

Stabilized

plus

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

Make rs121908898(G;T)

Make rs121908898(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

58146043

Gene

FLNB

is a	snp
is	mentioned by
dbSNP	rs121908898
dbSNP (classic)	rs121908898
ClinGen	rs121908898
ebi	rs121908898
HLI	rs121908898
Exac	rs121908898
Gnomad	rs121908898
Varsome	rs121908898
LitVar	rs121908898
Map	rs121908898
PheGenI	rs121908898
Biobank	rs121908898
1000 genomes	rs121908898
hgdp	rs121908898
ensembl	rs121908898
geneview	rs121908898
scholar	rs121908898
google	rs121908898
pharmgkb	rs121908898
gwascentral	rs121908898
openSNP	rs121908898
23andMe	rs121908898
SNPshot	rs121908898
SNPdbe	rs121908898
MSV3d	rs121908898
GWAS Ctlg	rs121908898

Max Magnitude

0

OMIM	603381
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121908898(T;T)
Alt	rs121908898(T;T)
Reference	Rs121908898(G;G)
Significance	Pathogenic
Disease	Spondylocarpotarsal synostosis syndrome
Variation	info
Gene	FLNB
CLNDBN	Spondylocarpotarsal synostosis syndrome
Reversed	0
HGVS	NC_000003.11:g.58131770G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006777.2,