Variant (rsID / SNP)

rs1562957

rs1562957 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NA, LOC105373750. Location: chromosome 2, position 175,637,578. The table records no clinical significance for this variant.

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Reference-table entries

NANot classified

Variant type: intergenic_region
Chromosome / position: 2:175637578
HGVS: NA,n.175637578G>A

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.