Variant (rsID / SNP)

rs375508949

rs375508949 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHAG. Location: chromosome 6, position 49,604,368. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RHAGPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 6:49604368
Cytoband: 6p12.3
HGVS: NM_000324.3(RHAG):c.157+1G>A
Allele change: Silent

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.