Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs199509194

RHD

rs199509194 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHD. Location: chromosome 1, position 25,611,101. Clinical significance in the table: no interpretation for the single variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

RHDOther
Clinical significance (as recorded)
no interpretation for the single variant
Variant type
single nucleotide variant
Chromosome / position
1:25611101
Cytoband
1p36.11
HGVS
NM_016124.6(RHD):c.186G>T (p.Leu62Phe)
Allele change
Silent

Associated conditions / phenotypes

Missense_L62F|Missense_L62F|Missense_L62F

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.