Variant "HBS1L:n.135419631A>G"
Search results: 4 records
Variant information
Gene:
Variant:
HBS1L:n.135419631A>G
Genomic location:
chr6:135419631(hg19)
HGVS:
SO Term | RefSeq |
---|---|
HBS1L-MYB:n.135419631A>G |
Alias:
HBS1L:rs9389268
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
4
Disorder:
2
Reference:
3
Effect type:
Expressivity(4)
Modifier effect:
Altered Hb F levels(1)
,Altered levels of fetalhemoglobin and pain crisis(1)
,Altered severity(1)
,Risk factor(1)
Details: