Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs61733105

GGCX

rs61733105 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GGCX. Location: chromosome 2, position 85,777,856. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

GGCXConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:85777856
Cytoband
2p11.2
HGVS
NM_000821.7(GGCX):c.1906C>A (p.Pro636Thr)
Allele change
Missense_P579T

Associated conditions / phenotypes

Vitamin K-dependent clotting factors, combined deficiency of, type 1

Public references

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