Variant (rsID / SNP)

rs6066

rs6066 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GP1BA. Location: chromosome 17, position 4,836,673. Clinical significance in the table: Benign.

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Reference-table entries

GP1BABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:4836673
Cytoband: 17p13.2
HGVS: NM_000173.7(GP1BA):c.774C>T (p.Asn258=)
Allele change: Synonymous_N258N

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.