Variant (rsID / SNP)

rs16879498

rs16879498 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHAG. Location: chromosome 6, position 49,580,247. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RHAGBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:49580247
Cytoband: 6p12.3
HGVS: NM_000324.3(RHAG):c.808G>A (p.Val270Ile)
Allele change: Missense_V270I

Associated conditions / phenotypes

Rh-null, regulator type

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.