Variant (rsID / SNP)

rs8176743

rs8176743 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABO. Location: chromosome 9, position 136,131,415. The table records no clinical significance for this variant.

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Reference-table entries

ABONot classified

Variant type: missense_variant
Chromosome / position: 9:136131415
HGVS: NM_020469.3,c.700G>A,p.Gly234Ser
Allele change: Synonymous_P234P

Associated conditions / phenotypes

Thrombophilia Due to Thrombin Defect|Thrombosis

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.