Variant (rsID / SNP)

rs61737314

rs61737314 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to H1-8. Location: chromosome 3, position 129,267,910. The table records no clinical significance for this variant.

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Reference-table entries

H1-8Not classified

Variant type: missense_variant
Chromosome / position: 3:129267910
HGVS: NM_153833.3,c.445G>A,p.Ala149Thr
Allele change: Missense_A149T

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.