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Variant (rsID / SNP)

rs11153361

RFPL4B

rs11153361 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RFPL4B. Location: chromosome 6, position 112,671,611. The table records no clinical significance for this variant.

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Reference-table entries

RFPL4BNot classified
Variant type
missense_variant
Chromosome / position
6:112671611
HGVS
NM_001013734.3,c.701G>A,p.Gly234Asp
Allele change
Missense_G234D

Public references

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