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rs34131035

From SNPedia

Merged intors863931
Orientationplus
Stabilizedplus
Make rs34131035(A;A)
Make rs34131035(A;G)
Make rs34131035(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position158642446
GeneSPTA1
is asnp
is mentioned by
dbSNPrs34131035
ebirs34131035
HLIrs34131035
Exacrs34131035
Varsomers34131035
Maprs34131035
PheGenIrs34131035
hapmaprs34131035
1000 genomesrs34131035
hgdprs34131035
ensemblrs34131035
gopubmedrs34131035
geneviewrs34131035
scholarrs34131035
googlers34131035
pharmgkbrs34131035
gwascentralrs34131035
openSNPrs34131035
23andMers34131035
23andMe allrs34131035
SNP Nexus

SNPshotrs34131035
SNPdbers34131035
MSV3drs34131035
GWAS Ctlgrs34131035
StatusMerged into rs863931
Max Magnitude
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene SPTA1
allele G
frequency
sift TOLERATED
HuRef 1103675236084
Disease Association Defects in SPTA1 are the cause of spherocytosis type III (SPH3) (MIM:270970). SPH3 is a disorder characterized by severe hemolytic anemia. Inheritance is autosomal recessive.