Have questions? Visit https://www.reddit.com/r/SNPedia

rs5036

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 2 Memphis variant of erythrocyte Band 3 glycoprotein
Make rs5036(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position44261577
GeneSLC4A1
is asnp
is mentioned by
dbSNPrs5036
dbSNP (classic)rs5036
ClinGenrs5036
ebirs5036
HLIrs5036
Exacrs5036
Gnomadrs5036
Varsomers5036
LitVarrs5036
Maprs5036
PheGenIrs5036
Biobankrs5036
1000 genomesrs5036
hgdprs5036
ensemblrs5036
geneviewrs5036
scholarrs5036
googlers5036
pharmgkbrs5036
gwascentralrs5036
openSNPrs5036
23andMers5036
SNPshotrs5036
SNPdbers5036
MSV3drs5036
GWAS Ctlgrs5036
GMAF0.06703
Max Magnitude2

aka c.166A>G (p.Lys56Glu or K56E)

This variant is known as the Memphis variant of the Band 3 glycoprotein, and it is found in perhaps 5-15% of individuals across various ethnicities. It is reported in ClinVar as likely to be benign, although some publications do cite some variation in anion transport in erythrocytes due to this (Memphis) variant.

? (A;A) (A;G) (G;G) 28


OMIM109270
DescBAND 3 MEMPHIS
Variant0001
Relatedalso



ClinVar
Risk rs5036(G;G)
Alt rs5036(G;G)
Reference Rs5036(A;A)
Significance Pathogenic
Disease Band 3 memphis not specified Hemolytic anemia Spherocytosis Distal Renal Tubular Acidosis
Variation info
Gene SLC4A1
CLNDBN Band 3 memphis not specified Hemolytic anemia Spherocytosis, Dominant Distal Renal Tubular Acidosis, Dominant
Reversed 1
HGVS NC_000017.10:g.42338945T>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000019328.30, RCV000251469.1, RCV000260217.1, RCV000300219.1, RCV000357412.1,