rs36006195

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs36006195(G;T)

Make rs36006195(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254725

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs36006195
dbSNP (classic)	rs36006195
ClinGen	rs36006195
ebi	rs36006195
HLI	rs36006195
Exac	rs36006195
Gnomad	rs36006195
Varsome	rs36006195
LitVar	rs36006195
Map	rs36006195
PheGenI	rs36006195
Biobank	rs36006195
1000 genomes	rs36006195
hgdp	rs36006195
ensembl	rs36006195
geneview	rs36006195
scholar	rs36006195
google	rs36006195
pharmgkb	rs36006195
gwascentral	rs36006195
openSNP	rs36006195
23andMe	rs36006195
SNPshot	rs36006195
SNPdbe	rs36006195
MSV3d	rs36006195
GWAS Ctlg	rs36006195

Max Magnitude

0

OMIM	142250
Desc
Variant	0013
Related	also

ClinVar
Risk	rs36006195(T;T)
Alt	rs36006195(T;T)
Reference	Rs36006195(G;G)
Significance	Other
Disease	HEMOGLOBIN F (MALAYSIA)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (MALAYSIA)
Reversed	1
HGVS	NC_000011.9:g.5275955C>A
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016109.1,

[PMID 4837284] Haemoglobin F Malaysia: alpha 2, gamma 2 1(NA1) glycine--cysteine; 136 glycine.