Variant (rsID / SNP)

rs104893987

rs104893987 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHAG. Location: chromosome 6, position 49,580,217. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

RHAGOther

Clinical significance (as recorded): no interpretation for the single variant
Variant type: single nucleotide variant
Chromosome / position: 6:49580217
Cytoband: 6p12.3
HGVS: NM_000324.3(RHAG):c.838G>A (p.Gly280Arg)
Allele change: Missense_G280R

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.