rs121908897

Orientation

plus

Stabilized

plus

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

Make rs121908897(C;T)

Make rs121908897(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

58148771

Gene

FLNB

is a	snp
is	mentioned by
dbSNP	rs121908897
dbSNP (classic)	rs121908897
ClinGen	rs121908897
ebi	rs121908897
HLI	rs121908897
Exac	rs121908897
Gnomad	rs121908897
Varsome	rs121908897
LitVar	rs121908897
Map	rs121908897
PheGenI	rs121908897
Biobank	rs121908897
1000 genomes	rs121908897
hgdp	rs121908897
ensembl	rs121908897
geneview	rs121908897
scholar	rs121908897
google	rs121908897
pharmgkb	rs121908897
gwascentral	rs121908897
openSNP	rs121908897
23andMe	rs121908897
SNPshot	rs121908897
SNPdbe	rs121908897
MSV3d	rs121908897
GWAS Ctlg	rs121908897

Max Magnitude

0

OMIM	603381
Desc
Variant	0013
Related	also

ClinVar
Risk	rs121908897(T;T)
Alt	rs121908897(T;T)
Reference	Rs121908897(C;C)
Significance	Pathogenic
Disease	Spondylocarpotarsal synostosis syndrome
Variation	info
Gene	FLNB
CLNDBN	Spondylocarpotarsal synostosis syndrome
Reversed	0
HGVS	NC_000003.11:g.58134498C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006776.2,