DSCAML1 c.512-118730A>G

Variant ID: 11-117521967-T-C

NM_020693.4(DSCAML1):c.512-118730A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Allelic variation in gene expression is common in the human genome.

Genome Research
Lo, H Shuen HS; Wang, Zhining Z; Hu, Ying Y; Yang, Howard H HH; Gere, Sheryl S; Buetow, Kenneth H KH; Lee, Maxwell P MP
Publication Date: 2003-08

Variant appearance in text: rs16867
PubMed Link: 12902379
Variant Present in the following documents:
  • Main text
View BVdb publication page